Immunotherapy of Cancer

ABSTRACT

Immunogenic modulators and compositions comprising oligonucleotide agents capable of inhibiting suppression of immune response by reducing expression of one or more gene involved with an immune suppression mechanism.

CROSS REFERENCE

This application claims priority to U.S. Provisional Application No. 61/910,728, filed Dec. 2, 2013, herein incorporated by reference in its entirety.

TECHNICAL FIELD

The present invention relates to immunogenic compositions, method of making immunogenic compositions, and methods of using immunogenic compositions for the treatment of cell proliferative disorders or infectious disease, including, for example, cancer and autoimmune disorders.

More particularly, the invention provides cells that are treated with oligonucleotides specifically designed to modulate expression of target genes involved in tumor immune resistance mechanisms.

BACKGROUND

Immunotherapy is the “treatment of disease by inducing, enhancing, or suppressing an immune response”. Immunotherapies designed to elicit or amplify an immune response are activation immunotherapies, while immunotherapies that reduce or suppress immune response are classified as suppression immunotherapies.

Immunotherapy of cancer has become increasingly important in clinical practice over recent decades. The primary approach in today's standard of care is passive immunotherapy through the use of recombinant monoclonal antibodies (mAbs). MAbs act through a mechanisms relevant to the body's own humoral immune response, by binding to key antigens involved in the tumor development and causing moderate forms of cell-mediated immunity, such as antibody-dependent cell-mediated cytotoxicity (ADCC).

Another group of emerging immunotherapeutic approaches is based on the administration of cells capable of destroying tumor cells. The administered cells may be the patient's own tumor-infiltrating lymphocytes (TIL), isolated and expanded ex-vivo. In some cases, TIL are capable of recognizing a variety of tumor associated antigens (TAA), while in other cases TIL can be reactivated and expanded in vitro to recognize specific antigens. The TIL-based therapeutic approaches are commonly referred to as “adoptive cell transfer” (ACT).

Further developments of ACT involve genetic modifications of T-cells to express receptors that recognize specific tumor-associated antigens (TAA). Such modifications may induce the expression of a specific T-cell receptor (TCR) or of a chimeric antigen receptor (CAR) consisting of TAA-specific antibody fused to CD3/co-stimulatory molecule transmembrane and cytoplasmic domains.

The ACT methods may also be considered as passive immunotherapeutic approaches in that they act directly on the tumor cells without invoking an extended immune response. However, unlike mAbs, ACT agents are capable of fully destroying the tumor cells, as opposed to the blockade of selected receptors and moderate cellular responses such as ADCC.

There is ongoing development of numerous methods of active immunotherapy, which restore the ability of body's own immune system to generate antitumor response. Active immunotherapeutic agents are often called therapeutic cancer vaccines, or just cancer vaccines. Many cancer vaccines are currently in clinical trials, and sipuleucell-T has recently become the first such vaccine approved by the United States FDA.

There are several classes of cancer vaccines using different antigens and different mechanisms of generating cell-mediated immune response. One class of vaccines is based on peptide fragments of antigens selectively expressed by tumor cells. The peptides are administered alone or in combination with immune-stimulatory agents, which may include adjuvants and cytokines, such as granulocyte-macrophage colony-stimulating factor (GM-CSF).

Another class of cancer vaccines is based on modified (e.g. sub-lethally irradiated) tumor cells used as antigens, also in combinations with immunostimulatory agents. Vaccines of this type currently in clinical trials are based both on autologous (e.g. OncoVAX, LipoNova) and allogeneic (e.g. Canvaxin, Onyvax-P, GVAX) tumor cell lines.

Yet another class of cancer vaccines uses dendritic cells. By their nature, dendritic cells (DC) are “professional” antigen-presenting cells capable of generating of a strong antigen-dependent cell-mediated immune response and eliciting therapeutic T-cells in vivo. DC-based cancer vaccines usually comprise DCs isolated from patients or generated ex vivo by culturing patient's hematopoietic progenitor cells or monocytes. DCs are further loaded with tumor antigens and sometimes combined with immune-stimulating agents, such as GM-CSF. A large number of DC-vaccines are now in clinical trials, and the first FDA-approved vaccine sipuleucell-T is based on DC.

Mechanisms of Immunosuppression and Therapeutic Approaches to its Mitigation

One of the key physiologic functions of the immune system is to recognize and eliminate neoplastic cells, therefore an essential part of any tumor progression is the development of immune resistance mechanisms. Once developed, these mechanisms not only prevent the natural immune system from effecting the tumor growth, but also limit the efficacy of any immunotherapeutic approaches to cancer. An important immune resistance mechanism involves immune-inhibitory pathways, sometimes referred to as immune checkpoints. The immune-inhibitory pathways play particularly important role in the interaction between tumor cells and CD8+ cytotoxic T-lymphocytes, including ACT therapeutic agents. Among important immune checkpoints are inhibitory receptors expressed on the T-cell surface, such as CTLA-4, PD1 and LAG3, among others.

The importance of the attenuation of immune checkpoints has been recognized by the scientific and medical community. One way to mitigate immunosuppression is to block the immune checkpoints by specially designed agents. The CTLA-4-blocking-antibody, ipilimumab, has recently been approved by the FDA. Several molecules blocking PD1 are currently in clinical development.

Immunosuppression mechanisms also negatively affect the function of dendritic cells and, as a consequence, the efficacy of DC-based cancer vaccines. Immunosuppressive mechanisms can inhibit the ability of DC to present tumor antigens through the MHC class I pathway and to prime naïve CD8+ T-cells for antitumor immunity. Among the important molecules responsible for the immunosuppression mechanisms in DC are ubiquitin ligase A20 and the broadly immune-suppressive protein SOCS1.

The efficacy of immunotherapeutic approaches to cancer can be augmented by combining them with inhibitors of immune checkpoints. Numerous ongoing preclinical and clinical studies are exploring potential synergies between cancer vaccines and other immunotherapeutic agents and checkpoint blocking agents, for example, ipilimumab. Such combination approaches have the potential to result in significantly improved clinical outcomes.

However, there are a number of drawbacks of using cancer immunotherapeutic agents in combination with checkpoint inhibitors. For example, immune checkpoint blockade can lead to the breaking of immune self-tolerance, thereby inducing a novel syndrome of autoimmune/auto-inflammatory side effects, designated “immune related adverse events,” mainly including rash, colitis, hepatitis and endocrinopathies (Corsello, et al. J. Clin. Endocrinol. Metab., 2013, 98:1361).

Reported toxicity profiles of checkpoint inhibitors are different than the toxicity profiles reported for other classes of oncologic agents. Those involve inflammatory events in multiple organ systems, including skin, gastrointestinal, endocrine, pulmonary, hepatic, ocular, and nervous system. (Hodi, 2013, Annals of Oncology, 24: Suppl, i7).

In view of the above, there is a need for new cancer therapeutic agents that can be used in combination with checkpoint inhibitors as well as other classes of oncolytic agents without risk of adverse inflammatory events in multiple organ systems previously reported for checkpoint inhibitors. The immunotherapeutic cells of the invention, prepared by treating cells with a combination oligonucleotide agents targeting genes associated with tumor or infections disease resistance mechanisms, as well as methods of producing such therapeutic cells and methods of treating disease with the produced therapeutic cells, satisfy this long felt need.

SUMMARY OF EMBODIMENTS OF THE INVENTION

The efficacy of immunotherapeutic approaches to cell proliferation disorders and infectious diseases can be augmented by combining them with inhibitors of immune checkpoints. Numerous synergies between cancer vaccines and other immunotherapeutic agents and checkpoint blocking agents provide opportunities for combination approaches that may significantly improve clinical outcomes for example, in proliferative cell disorders and immune diseases.

Various embodiments of the inventions disclosed herein include compositions comprising therapeutic cells obtained by treating cells ex vivo with oligonucleotides to modulate expression of target genes involved in immune suppression mechanisms. The oligonucleotide agent may be an antisense oligonucleotide (ASO), including locked nucleic acids (LNAs), methoxyethyl gapmers, and the like, or an siRNA, miRNA, miRNA-inhibitor, morpholino, PNA, and the like. The oligonucleotide is preferably a self-delivered (sd) RNAi agent. The oligonucleotides may be chemically modified, for example, including at least one 2-O-methyl modification, 2′-Fluro modification, and/or phosphorothioate modification. The oligonucleotides may include one or more hydrophobic modification, for example, one or more sterol, cholesterol, vitamin D, Naphtyl, isobutyl, benzyl, indol, tryptophane, or phenyl hydrophobic modification. The oligonucleotide may be a hydrophobically-modified siRNA-antisense hybrid. The oligonucleotides may be used in combination with transmembrane delivery systems, such as delivery systems comprising lipids.

In an embodiment, the cells are obtained and/or derived from a cancer or infectious disease patient, and may be, for example, tumor infiltrating lymphocytes (TIL) and/or T-cells, antigen presenting cells such as dendritic cells, natural killer cells, induced-pluripotent stem cells, stem central memory T-cells, and the like. The T-cells and NK-cells are preferably genetically engineered to express high-affinity T-Cell receptors (TCR) and/or chimeric antibody or antibody-fragment-T-Cell receptors (CAR). In an embodiment, the chimeric antibody/antibody fragment is preferably capable of binding to antigens expressed on tumor cells. Immune cells may be engineered by transfection with plasmid, viral delivery vehicles, or mRNAs.

In an embodiment, the chimeric antibody or fragment is capable of binding CD19 receptors of B-cells and/or binding to antigens expressed on tumors, such as melanoma tumors. Such melanoma-expressed antigens include, for example, GD2, GD3, HMW-MAA, VEGF-R2, and the like.

Target genes identified herein for modification include: cytotoxic T-cell antigen 4 (CTLA4), programmed cell death protein 1 (PD1), tumor growth factor receptor beta (TGFR-beta), LAG3, TIM3, and adenosine A2a receptor; anti-apoptotic genes including, but not limited to: BAX, BAC, Casp8, and P53; A20 ubiquitine ligase (TNFAIP3, SOCS1 (suppressor of cytokine signaling), IDO (indolamine-2,3-dioxygenase; tryptophan-degrading enzyme), PD-L1 (CD274)(surface receptor, binder to PD1 on Tcells), Notch ligand Delta1 (DLL1), Jagged 1, Jagged 2, FasL (pro-apoptotic surface molecule), CCL17, CCL22 (secreted chemokines that attract Treg cells), IL10 receptor (IL10RA), p38 (MAPK14), STAT3, TNFSF4 (OX40L), MicroRNA miR-155, miR-146a, anti-apoptotic genes including but not limited to BAX, BAC, Casp8 and P53, and the like genes, and combinations thereof. Representative target sequences are listed in Table 1.

The engineered therapeutic cells are treated with RNAi agents designed to inhibit expression of one or more of the targeted genes. The RNAi agent may comprise a guide sequence that hybridizes to a target gene and inhibits expression of the target gene through an RNA interference mechanism, where the target region is selected from the group listed in Table 1. The RNA agent can be chemically modified, and preferably includes at least one 2′-O-methyl, 2′-O-Fluoro, and/or phosphorothioate modification, as well as at least one hydrophobic modification such as cholesterol, and the like.

The immunogenic compositions described herein are useful for the treatment of proliferative disorders, including cancers, and/or infectious disease and are produced by the ex-vivo treatment of cells with oligonucleotides to modulate the expression of target genes involved in tumor immune resistance mechanisms. The ex vivo treatment of cells includes administering to the cells an oligonucleotide capable of targeting and inhibiting expression of a gene involved in a tumor suppressor mechanism, such as the genes listed in Table 1. The oligonucleotide can be used in combination with a transmembrane delivery system that may comprise one or more of: lipid(s) and vector, such as a viral vector.

The invention includes a method of treating a cell proliferative disorder or infectious disease by administering to a subject in need thereof, an immunogenic composition comprising cells that have been treated with one or more oligonucleotide to modulate the expression of one or more target gene involved in tumor immune resistance mechanisms, for example, one or more of the target genes of Table 1.

The invention preferably includes immunogenic cells treated with a plurality of oligonucleotide agents targeting a combination of target genes described herein. The combination may target a plurality of suppressor receptor genes, cytokine receptor genes, regulatory genes, and/or apoptotic factors in order to inhibit tumor immune resistance mechanisms.

The present invention is directed to novel immunotherapeutic cells, methods of generating the immunotherapeutic cells, and therapeutic methods employing such cells.

A new method of immune checkpoint inhibition is described herein, applicable to a broad variety of cell-based immunotherapies, including, but not limited to adaptive cell transfer, for example, based on TIL, TCR, CAR, and other cell types, as well as dendritic cell-based cancer vaccines. Self-deliverable RNAi technology provides efficient transfection of short oligonucleotides in any cell type, including immune cells, providing increased efficacy of immunotherapeutic treatments. In addition, the activated immune cells can be protected by preventing apoptosis via inhibition of key activators of the apoptotic pathway, such as BAC, BAX, Casp8, and P53, among others.

The activated immune cells modified by oligonucleotide transfer for a single therapeutic agent for administration to a subject, providing a number of advantages as compared to separately administered combinations of vaccines and immunotherapeutics and separately administered checkpoint inhibitors. These advantages include lack of side effects associated with the checkpoint inhibitors in a single therapeutic agent (activated immune cells modified by oligonucleotides targeting immune resistance genes).

The claimed immunotherapeutic cells, method of producing immunotherapeutic cells by introduction of oligonucleotide molecules targeting immune resistance pathways, and methods of treating proliferative and infectious disease, improves upon any known immunotherapeutic cells and methods of producing immunotherapeutic cells because it provides:

-   -   1) a single therapeutic composition providing a combination of         checkpoint inhibitors and other immune resistance mechanism         inhibitors;     -   2) with reduced toxicity; and     -   3) increased efficacy as compared with other compositions.

BRIEF DESCRIPTION OF THE FIGURES

The foregoing features of embodiments will be more readily understood by reference to the following detailed description, taken with reference to the accompanying drawings, in which:

FIG. 1 is a schematic diagram showing the structure of an sdRNA molecule.

FIG. 2 is a graph showing sdRNA-induced silencing of GAPDH and MAP4K4 in HeLa cells.

FIG. 3 is a graph showing sdRNA-induced knock-down of multiple targets using sdRNA agents directed to three genes in NK-92 cells.

FIG. 4 is a graph showing the knock-down of gene expression in Human Primary T cells by sdRNA agents targeting TP53 and MAP4K4.

FIG. 5 is a graph showing sdRNA-induced knock-down of CTLA4 and PD1 in Human Primary T cells.

FIG. 6 is a graph showing the reduction of PDCD1 and CTLA-4 surface expression by sdRNA in Human Primary T cells.

FIG. 7 is a graph showing MAP4K4-cy3 sdRNA delivery into T and B cells in human PBMCs.

DETAILED DESCRIPTION OF SPECIFIC EMBODIMENTS

The invention is defined by the claims, and includes oligonucleotides specifically designed and selected to reduce and/or inhibit expression of suppressors of immune resistance (inhibitory oligonucleotides), compositions comprising cells modified by treatment with such inhibitory oligonucleotides, methods of making such compositions, and methods of using the compositions to treat proliferation and/or infectious diseases. In particular, cells are treated with a combination of oligonucleotide agents, each agent particularly designed to interfere with and reduce the activity of a targeted immune suppressor.

Preferably, the combination of oligonucleotide agents targets multiple immune suppressor genes selected from checkpoint inhibitor genes such as CTLA4, PD-1/PD-1L, BTLA (B and T-lymphocyte attenuator), KIR (killer immunoglobulin-like receptors), B7-H3, B7-H4 receptors, and TGF beta type 2 receptor; cytokine receptors that inactivate immune cells, such as TGF-beta receptor A and IL-10 receptor; regulatory genes/transcription factors modulating cytokine production by immune cells, such as STAT-3 and P38, miR-155, miR-146a; and apoptotic factors involved in cascades leading to cell death, such as p53 and Cacp8.

Most preferably the oligonucleotide agent is a self-deliverable RNAi agent, which is a hydrophobically modified siRNA-antisense hybrid molecule, comprising a double-stranded region of about 13-22 base pairs, with or without a 3′-overhang on each of the sense and antisense strands, and a 3′ single-stranded tail on the antisense strand of about 2-9 nucleotides. The oligonucleotide contains at least one 2′-O-Methyl modification, at least one 2′-O-Fluoro modification, and at least one phosphorothioate modification, as well as at least one hydrophobic modification selected from sterol, cholesterol, vitamin D, napthyl, isobutyl, benzyl, indol, tryptophane, phenyl, and the like hydrophobic modifiers (see FIG. 1). The oligonucleotide may contain a plurality of such modifications.

DEFINITIONS

As used in this description and the accompanying claims, the following terms shall have the meanings indicated, unless the context requires otherwise:

Proliferative disease, as used herein, includes diseases and disorders characterized by excessive proliferation of cells and turnover of cellular matrix, including cancer, atherlorosclerosis, rheumatoid arthritis, psoriasis, idiopathic pulmonary fibrosis, scleroderma, cirrhosis of the liver, and the like. Cancers include but are not limited to, one or more of: small cell lung cancer, colon cancer, breast cancer, lung cancer, prostate cancer, ovarian cancer, pancreatic cancer, melanoma, hematological malignancy such as chronic myeloid leukemia, and the like cancers where immunotherapeutic intervention to suppress tumor related immune resistance is needed.

Immune target genes can be grouped into at least four general categories: (1) checkpoint inhibitors; (2) cytokine receptors that inactivate immune cells, (3) anti-apoptotic genes; and (4) regulator genes, for example, transcription factors.

Immune Checkpoint inhibitors (ICI), as used herein, include immunotherapeutic agents that bind to certain checkpoint proteins, such as cytotoxic T lymphocyte antigen-4 (CTLA-4) and programmed death-1 (PD-1) and its ligand PD-L1 to block and disable inhibitory proteins that prevent the immune system from attacking diseased cells such as cancer cells, liberating tumor-specific T cells to exert their effector function against tumor cells.

Tumor related immune resistance genes, as used herein, include genes involved in checkpoint inhibition of immune response, such as CTLA-4 and PD-1/PD-L1; TGF-beta, LAG3, Tim3, adenosine A2a receptor;

Regulator genes, as used herein, include transcription factors and the like that modulate cytokine production by immune cells, and include p38, STAT3, microRNAs miR-155, miR-146a;

Anti-apoptotic genes, as used herein, include BAX, BAC, Casp8, P53 and the like; and combinations thereof.

Infectious diseases, as used herein, include, but are not limited to, diseases caused by pathogenic microorganisms, including, but not limited to, one or more of bacteria, viruses, parasites, or fungi, where immunotherapeutic intervention to suppress pathogen related immune resistance and/or overactive immune response.

Immunogenic composition, as used herein, includes cells treated with one or more oligonucleotide agent, wherein the cells comprise T-cells. The T-cells may be genetically engineered, for example, to express high affinity T-cell receptors (TCR), chimeric antibody-T-cell receptors (CAR), where the chimeric antibody fragments are capable of binding to CD19 receptors of B-cells and/or to antigens expressed on tumor cells. In one embodiment, the chimeric antibody fragments bind antigens expressed on melanoma tumors, selected from GD2, GD3, HMW-MAA, and VEGF-R2.

Immunogenic compositions described herein include cells comprising antigen-presenting cells, dendritic cells, engineered T-cells, natural killer cells, stem cells, including induced pluripotent stem cells, and stem central memory T-cells. The treated cell also comprises one or a plurality of oligonucleotide agents, preferably sdRNAi agents specifically targeting a gene involved in an immune suppression mechanism, where the oligonucleotide agent inhibits expression of said target gene.

In one embodiment, the target gene is selected from A20 ubiquitin ligase such as TNFAIP3, SOCS1 (suppressor of cytokine signaling), Tyro3/Ax1/Mer (suppressors of TLR signaling), IDO (indolamine-2,3-dioxygenase, tryptophan-degrading enzyme), PD-L1/CD274 (surface receptor, binds PD1 on T-cells), Notch ligand Delta (DLL1), Jagged 1, Jagged 2, FasL (pro-apoptotic surface molecule), CCL17, CCL22 (secreted chemokines that attract Treg cells), IL-10 receptor (IL10Ra), p38 (MAPK14), STAT3, TNFSF4 (OX40L), microRNA miR-155, miR-146a, anti-apoptotic genes, including but not limited to BAX, BAC, Casp8, and P53; and combinations thereof.

Particularly preferred target genes are those shown in Table 1.

Ex-vivo treatment, as used herein, includes cells treated with oligonucleotide agents that modulate expression of target genes involved in immune suppression mechanisms. The oligonucleotide agent may be an antisense oligonucleotide, including, for example, locked nucleotide analogs, methyoxyethyl gapmers, cyclo-ethyl-B nucleic acids, siRNAs, miRNAs, miRNA inhibitors, morpholinos, PNAs, and the like. Preferably, the oligonucleotide agent is an sdRNAi agent targeting a gene involved in an immune suppression mechanism. The cells treated in vitro by the oligonucleotide agent may be immune cells expanded in vitro, and can be cells obtained from a subject having a proliferative or infectious disease. Alternatively, the cells or tissue may be treated in vivo, for example by in situ injection and/or intravenous injection.

Oligonucleotide or oligonucleotide agent, as used herein, refers to a molecule containing a plurality of “nucleotides” including deoxyribonucleotides, ribonucleotides, or modified nucleotides, and polymers thereof in single- or double-stranded form. The term encompasses nucleotides containing known nucleotide analogs or modified backbone residues or linkages, which are synthetic, naturally occurring, and non-naturally occurring, which have similar binding properties as the reference nucleic acid, and which are metabolized in a manner similar to the reference nucleotides. Examples of such analogs include, without limitation, phosphorothioates, phosphoramidates, methyl phosphonates, chiral-methyl phosphonates, 2-O-methyl ribonucleotides, peptide-nucleic acids (PNAs).

Nucleotide, as used herein to include those with natural bases (standard), and modified bases well known in the art. The nucleotides can be unmodified or modified at the sugar, phosphate and/or base moiety, (also referred to interchangeably as nucleotide analogs, modified nucleotides, non-natural nucleotides, non-standard nucleotides and other; see, for example, PCT Publications No. WO 92/07065 and WO 93/15187. Non-limiting examples of base modifications that can be introduced into nucleic acid molecules include, hypoxanthine, purine, pyridin-4-one, pyridin-2-one, phenyl, pseudouracil, 2,4,6-trimethoxy benzene, 3-methyl uracil, dihydrouridine, naphthyl, aminophenyl, 5-alkylcytidines (e.g., 5-methylcytidine), 5-alkyluridines (e.g., ribothymidine), 5-halouridine (e.g., 5-bromouridine) or 6-azapyrimidines or 6-alkylpyrimidines (e.g. 6-methyluridine and pseudouridine), propyne, and others. The phrase “modified bases” includes nucleotide bases other than adenine, guanine, cytosine, and uracil, modified for example, at the 1′ position or their equivalents.

As used herein, the term “deoxyribonucleotide” encompasses natural and synthetic, unmodified and modified deoxyribonucleotides. Modifications include changes to the sugar moiety, to the base moiety and/or to the linkages between deoxyribonucleotide in the oligonucleotide.

As used herein, the term “RNA” defines a molecule comprising at least one ribonucleotide residue. The term “ribonucleotide” defines a nucleotide with a hydroxyl group at the 2′ position of a b-D-ribofuranose moiety. The term RNA includes double-stranded RNA, single-stranded RNA, isolated RNA such as partially purified RNA, essentially pure RNA, synthetic RNA, recombinantly produced RNA, as well as altered RNA that differs from naturally occurring RNA by the addition, deletion, substitution and/or alteration of one or more nucleotides. Nucleotides of the RNA molecules described herein may also comprise non-standard nucleotides, such as non-naturally occurring nucleotides or chemically synthesized nucleotides or deoxynucleotides. These altered RNAs can be referred to as analogs or analogs of naturally-occurring RNA.

As used herein, “modified nucleotide” refers to a nucleotide that has one or more modifications to the nucleoside, the nucleobase, pentose ring, or phosphate group. For example, modified nucleotides exclude ribonucleotides containing adenosine monophosphate, guanosine monophosphate, uridine monophosphate, and cytidine monophosphate and deoxyribonucleotides containing deoxyadenosine monophosphate, deoxyguanosine monophosphate, deoxythymidine monophosphate, and deoxycytidine monophosphate. Modifications include those naturally-occurring that result from modification by enzymes that modify nucleotides, such as methyltransferases.

Modified nucleotides also include synthetic or non-naturally occurring nucleotides. Synthetic or non-naturally occurring modifications in nucleotides include those with 2′ modifications, e.g., 2′-O-methyl, 2′-methoxyethoxy, 2′-fluoro, 2′-allyl, 2′-O-[2-(methylamino)-2-oxoethyl], 4′-thio, 4′-CH2-O-2′-bridge, 4′-(CH2) 2-O-2′-bridge, 2′-LNA, and 2′-O—(N-methylcarbamate) or those comprising base analogs. In connection with 2′-modified nucleotides as described for the present disclosure, by “amino” is meant 2′-NH2 or 2′-O—NH2, which can be modified or unmodified. Such modified groups are described, for example, in U.S. Pat. Nos. 5,672,695 and 6,248,878.

As used herein, “microRNA” or “miRNA” refers to a nucleic acid that forms a single-stranded RNA, which single-stranded RNA has the ability to alter the expression (reduce or inhibit expression; modulate expression; directly or indirectly enhance expression) of a gene or target gene when the miRNA is expressed in the same cell as the gene or target gene. In one embodiment, a miRNA refers to a nucleic acid that has substantial or complete identity to a target gene and forms a single-stranded miRNA. In some embodiments miRNA may be in the form of pre-miRNA, wherein the pre-miRNA is double-stranded RNA. The sequence of the miRNA can correspond to the full length target gene, or a subsequence thereof. Typically, the miRNA is at least about 15-50 nucleotides in length (e.g., each sequence of the single-stranded miRNA is 15-50 nucleotides in length, and the double stranded pre-miRNA is about 15-50 base pairs in length). In some embodiments the miRNA is 20-30 base nucleotides. In some embodiments the miRNA is 20-25 nucleotides in length. In some embodiments the miRNA is 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or 30 nucleotides in length.

Target gene, as used herein, includes genes known or identified as modulating the expression of a gene involved in an immune resistance mechanism, and can be one of several groups of genes, such as suppressor receptors, for example, CTLA4 and PD1; cytokine receptors that inactivate immune cells, for example, TGF-beta receptor, LAG3, Tim3, adenosine A2a receptor, and IL10 receptor; regulatory genes for example, STAT3, p38, mir155 and mir146a; and apoptosis factors involved in cascades leading to cell death, for example, P53, Casp8, BAX, BAC, and combinations thereof. See also preferred target genes listed in Table 1.

As used herein, small interfering RNA (siRNA), sometimes known as short interfering RNA or silencing RNA, defines a group of double-stranded RNA molecules, comprising sense and antisense RNA strands, each generally of about 1022 nucleotides in length, optionally including a 3′ overhang of 1-3 nucleotides. siRNA is active in the RNA interference (RNAi) pathway, and interferes with expression of specific target genes with complementary nucleotide sequences.

As used herein, sdRNA refers to “self-deliverable” RNAi agents, that are formed as an asymmetric double-stranded RNA-antisense oligonucleotide hybrid. The double stranded RNA includes a guide (sense) strand of about 19-25 nucleotides and a passenger (antisense) strand of about 10-19 nucleotides with a duplex formation that results in a single-stranded phosphorothiolated tail of about 5-9 nucleotides.

The RNA sequences may be modified with stabilizing and hydrophobic modifications such as sterols, for example, cholesterol, vitamin D, naphtyl, isobutyl, benzyl, indol, tryptophane, and phenyl, which confer stability and efficient cellular uptake in the absence of any transfection reagent or formulation. Immune response assays testing for IFN-induced proteins indicate sdRNAs produce a reduced immunostimulatory profile as compared other RNAi agents. See, for example, Byrne et al., December 2013, J. Ocular Pharmacology and Therapeutics, 29(10): 855-864.

Cell-Based Immunotherapeutics

In general, cells are obtained from subjects with proliferative disease such as cancer, or an infectious disease such as viral infection. The obtained cells are treated directly as obtained or may be expanded in cell culture prior to treatment with oligonucleotides. The cells may also be genetically modified to express receptors that recognize specific antigens expressed on the tumor cell surface (CAR) or intracellular tumor antigens presented on MHC class I (TCR).

Oligonucleotide Agents Antisense Oligonucleotides

Small interfering RNA (siRNA), sometimes known as short interfering RNA or silencing RNA, is a double stranded RNA molecule, generally 19-25 base pairs in length. siRNA is used in RNA interference (RNAi), where it interferes with expression of specific genes with complementary nucleotide sequences.

Double stranded DNA (dsRNA) can be generally used to define any molecule comprising a pair of complementary strands of RNA, generally a sense (passenger) and antisense (guide) strands, and may include single-stranded overhang regions. The term dsRNA, contrasted with siRNA, generally refers to a precursor molecule that includes the sequence of an siRNA molecule which is released from the larger dsRNA molecule by the action of cleavage enzyme systems, including Dicer.

sdRNA (self-deliverable) are a new class of covalently modified RNAi compounds that do not require a delivery vehicle to enter cells and have improved pharmacology compared to traditional siRNAs. “Self-deliverable RNA” or sdRNA is a hydrophobically modified RNA interfering-antisense hybrid, demonstrated to be highly efficacious in vitro in primary cells and in vivo upon local administration. Robust uptake and/or silencing without toxicity has been demonstrated in several tissues including dermal, muscle, tumors, alveolar macrophages, spinal cord, and retina cells and tissues. In dermal layer and retina, intradermal and intra-vitreal injection of sdRNA at mg doses induced potent and long lasting silencing.

While sdRNA is a superior functional genomics tool, enabling RNAi in primary cells and in vivo, it has a relatively low hit rate as compared to conventional siRNAs. While the need to screen large number of sequences per gene is not a limiting factor for therapeutic applications, it severely limits the applicability of sdRNA technology to functional genomics, where cost effective compound selection against thousands of genes is required. To optimize sdRNA structure, chemistry, targeting position, sequence preferences, and the like, a proprietary algorithm has been developed and utilized for sdRNA potency prediction. Availability of sdRNA reagents that are active in all cell types ex vivo and in vivo enables functional genomics and target stratification/validation studies.

Proprietary Algorithm

SdRNA sequences were selected based on a proprietary selection algorithm, designed on the basis of a functional screen of over 500 sdRNA sequences in the luciferase reporter assay of HeLa cells. Regression analysis of was used to establish a correlation between the frequency of occurrence of specific nucleotide and modification at any specific position in sdRNA duplex and its functionality in gene suppression assay. This algorithm allows prediction of functional sdRNA sequences, defined as having over 70% knockdown at 1 μM concentration, with a probability over 40%.

Table 1 shows predictive gene targets identified using the proprietary algorithm and useful in the cellular immunotherapeutic compositions and methods described herein.

Delivery of RNAi Agents

BTLA (B and T-lymphocyte attenuator), KIR (killer immunoglobulin-like receptors), B7-H3 and B7-H4 receptors and TGFbeta type 2 receptor; Applic BTLA (B and T-lymphocyte attenuator), KIR (killer immunoglobulin-like receptors), B7-H3 and B7-H4 receptors and TGFbeta type 2 receptor; ation of RNAi technology to functional genomics studies in prim BTLA (B and T-lymphocyte attenuator), KIR (killer immunoglobulin-like receptors), B7-H3 and B7-H4 receptors and TGFbeta type 2 receptor; ary cells and in vivo is limited by requirements to formulate siRNAs into lipids or use of other cell delivery techniques. To circumvent delivery problems, the self-deliverable RNAi technology provides a method of directly transfecting cells with the RNAi agent, without the need for additional formulations or techniques. The ability to transfect hard-to-transfect cell lines, high in vivo activity, and simplicity of use, are characteristics of the compositions and methods that present significant functional advantages over traditional siRNA-based techniques. The sdRNAi technology allows direct delivery of chemically synthesized compounds to a wide range of primary cells and tissues, both ex-vivo and in vivo.

To enable BTLA (B and T-lymphocyte attenuator), MR (killer immunoglobulin-like receptors), B7-H3 and B7-H4 receptors and TGFbeta type 2 receptor; self-delivery, traditional siRNA molecules require a substantial reduction in size and the introduction of extensive chemical modifications which are not well tolerated by RNAi machinery, resulting in extremely low probability of finding active molecules (low hit rate). In contrast, the sdRNA technology allows efficient RNAi delivery to primary cells and tissues in vitro and in vivo, with demonstrated silencing efficiency in humans.

The general structure of sdRNA molecules is shown in FIG. 1. sdRNA are formed as hydrophobically-modified siRNA-antisense oligonucleotide hybrid structures, and are disclosed, for example in Byrne et al., December 2013, J. Ocular Pharmacology and Therapeutics, 29(10): 855-864.

Oligonucleotide Modifications: 2′-O-methyl, 2′-O-Fluro, phosphorothioate

The oligonucleotide agents preferably comprise one or more modification to increase stability and/or effectiveness of the therapeutic agent, and to effect efficient delivery of the oligonucleotide to the cells or tissue to be treated. Such modifications include at least one

BTLA (B and T-lymphocyte attenuator), KIR (killer immunoglobulin-like receptors), B7-H3 and B7-H4 receptors and TGFbeta type 2 receptor; BTLA (B and T-lymphocyte attenuator), KIR (killer immunoglobulin-like receptors), B7-H3 and B7-H4 receptors and TGFbeta type 2 receptor; 2′-O-methyl modification, at least one 2′-O-Fluro modification, and at least one diphosphorothioate modification. Additionally, the oligonucleotide is modified to include one or more hydrophobic modification selected from sterol, cholesterol, vitamin D, naphtyl, isobutyl, benzyl, indol, tryptophane, and phenyl. The hydrophobic modification is preferably a sterol.

Delivery of Oligonucleotide Agents to Cells

The oligonucleotides may be delivered to the cells in combination with a transmembrane delivery system, preferably comprising lipids, viral vectors, and the like. Most preferably, the oligonucleotide agent is a self-delivery RNAi agent, that does not require any delivery agents.

Combination Therapy

Most preferred for this invention, e.g. particular combinations of elements and/or alternatives for specific needs. This objective is accomplished by determining the appropriate genes to be targeted by the oligonucleotide in order to silence immune suppressor genes and using the proprietary algorithm to select the most appropriate target sequence.

It is preferred that the immunotherapeutic cell be modified to include multiple oligonucleotide agents targeting a variety of genes involved in immune suppression and appropriate for the selected target disease and genes. For example, a preferred immunotherapeutic cell is a T-Cell modified to knock-down both CTLA-4 and PD-1

Additional combinations of oligonucleotides to related genes involved in immune suppression include varied combinations of the selected target sequences of Table 1.

BTLA (B and T-lymphocyte attenuator), MR (killer immunoglobulin-like receptors), B7-H3 and B7-H4 receptors and TGFbeta type 2 receptor; (B and T-lymphocyte attenuator), MR (killer immunoglobulin-like receptors), B7-H3 and B7-H4 receptors and TGFbeta type 2 receptor; Preferred BTLA (B and T-lymphocyte attenuator), KIR (killer immunoglobulin-like receptors), B7-H3 and B7-H4 receptors and TGFbeta type 2 receptor; therapeutic combinations include cells engineered to knock down gene expression of the following target genes:

a) CTLA4 and PD1

b) STAT3 and p38

c) PD1 and BaxPD1, CTLA4, Lag-1, ILM-3, and TP53

d) PD1 and Casp8

e) PD1 and IL10R

The therapeutic compositions described herein are useful to treat a subject suffering from a proliferation disorder or infectious disease. In particular, the immunotherapeutic composition is useful to treat disease characterized by suppression of the subjects immune mechanisms. The sdRNA agents described herein are specifically designed to target genes involved in diseases-associated immune suppression pathways.

Methods of treating a subject comprise administering to a subject in need thereof, an immunogenic composition comprising an sdRNAi agent capable of inhibiting expression of genes involved in immune suppression mechanisms, for example, any of the genes listed in Table 1 or otherwise described herein.

EXAMPLES

The embodiments of the invention described above are intended to be merely exemplary; numerous variations and modifications will be apparent to those skilled in the art. All such variations and modifications are intended to be within the scope of the present invention as defined in any appended claims.

Example 1 Self-Deliverable RNAi Immunotherapeutic Agents

Immunotherapeutic agents described herein were produced by treating cells with particular sdRNA agents designed to target and knock down specific genes involved in immune suppression mechanisms. In particular, the following cells and cell lines have been successfully treated with sdRNA and were shown to knock down at least 70% of targeted gene expression in the specified human cells.

These studies demonstrated utility of these immunogenic agents to suppress expression of target genes in cells normally very resistant to transfection, and suggests the agents are capable of reducing expression of target cells in any cell type.

TABLE 2 Target Cell Type Gene sdRNA target sequence % Knock Down Primary human TP53 (P53) GAGTAGGACATACCAGCTTA >70% 2 uM T-cells Primary human MAP4K4 AGAGTTCTGTGGAAGTCTA >70% 2 uM T-cells Jurkat T-lymphoma MAP4K4 AGAGTTCTGTGGAAGTCTA 100% 1 uM 72h cells NK-92 cells MAP4K4 AGAGTTCTGTGGAAGTCTA  80% 2 uM 72h NK-92 cells PPIB ACAGCAAATTCCATCGTGT >75% 2 uM 72h NK-92 cells GADPH CTGGTAAAGTGGATATTGTT >90% 2 uM 72h HeLa Cells MAP4K4 AGAGTTCTGTGGAAGTCTA >80% 2 uM 72h

Example 2 Oligonucleotide Sequences for Inhibiting Expression of Target Genes

A number of human genes were selected as candidate target genes due to involvement in immune suppression mechanisms, including the following genes:

BAX BAK1 CASP8 (NM_004324) (NM_001188) (NM_001228) ADORA2A CTLA4 LAG3 (NM_000675) (NM_005214) (NM002286) PDCD1 TGFBR1 HAVCR2 (NM_NM005018) (NM-004612) (NM_032782) CCL17 CCL22 DLL2 (NM_002987) (NM_002990) (NM_005618) FASLG CD274 IDO1 (NM_000639) (NM_001267706) (NM_002164) IL10RA JAG1 JAG2 (NM_001558) (NM_000214) (NM_002226) MAPK14 SOCS1 STAT3 (NM_001315) (NM_003745) (NM_003150) TNFA1P3 TNFSF4 TYRO2 (NM_006290) (NM_003326) (NM_006293) TP53 (NM_000546)

Each of the genes listed above was analyzed using a proprietary algorithm to identify preferred sdRNA targeting sequences and target regions for each gene for prevention of immunosuppression of antigen-presenting cells and T-cells. Results are shown in Table 1.

Example 3 Knock-Down of Target Gene (GAPDH) by sdRNA in HeLa Cells

HeLa cells (ATCC CRM-CCL-2) were subcultured 24 hours before transfection and kept log phase. The efficacy of several GAPDH sdRNAs was tested by qRT-PCR, including G13 sdRNA listed in the Table 1.

Solutions of GAPDH, MAP4K4 (positive control) and NTC (non-targeting control) sdRNA with twice the required concentration were prepared in serum-free EMEM medium, by diluting 100 μM oligonucleotides to 0.2-4 μM.

The total volume of medium for each oligo concentration point was calculated as [50 μl/well]×[number of replicates for each serum point]. Oligonucleotides were dispensed into a 96 well plate at 50 μl/well.

Cells were collected for transfection by trypsinization in a 50 ml tube, washed twice with medium containing 10% FBS without antibiotics, spun down at 200×g for 5 minutes at room temperature and resuspended in EMEM medium containing twice the required amount of FBS for the experiment (6%) and without antibiotics. The concentration of the cells was adjusted to 120,000/ml to yield a final concentration of 6,000 cells/50 μl/well. The cells were dispensed at 50 μl/well into the 96-well plate with pre-diluted oligos and placed in the incubator for 48 hours.

Gene Expression Analysis in HeLa Cells Using qRT-PCR

RNA was isolated from transfected HeLa cells using the PureLink™ Pro96 total RNA purification Kit (Ambion, Cat. No. 12173-011A), with Quanta qScript XLT One-Step RT-qPCR ToughMix, ROX (VWR, 89236672). The isolated RNA was analyzed for gene expression using the Human MAP4K4-FAM (Taqman Hs0377405_ml) and Human GAPDH-VIC (Applied Biosystems, Cat. No. 4326317E) gene expression assays.

The incubated plate was spun down and washed once with 100 μl/well PBS and lysed with 60 μl/well buffer provided in the kit. RNA isolation was conducted according to the manufacturer's instructions, and the RNA was eluted with 100 μl RNase-free water, and used undiluted for one-step qRT-PCR.

Dilutions of non-transfected (NT) cells of 1:5 and 1:25 were prepared for the standard curve using RNase-free water. qRT-PCR was performed by dispensing 9 μl/well into a low profile PCR plate and adding 1 μl RNA/well from the earlier prepared RNA samples. After brief centrifugation, the samples were placed in the real-time cycler and amplified using the settings recommended by the manufacturer.

GAPDH gene expression was measured by qPCR, normalized to MAP4K4 and plotted as percent of expression in the presence of non-targeting sdRNA. The results were compared to the normalized according to the standard curve. As shown in FIG. 2, several sdRNA agents targeting GAPDH or MAP4K4 significantly reduced their mRNA levels leading to more than 80-90% knock-down with 1 μM sdRNA. (See FIG. 2).

Example 4 Silencing of Multiple Targets by sdRNA in NK-92 Cells

NK-92 cells were obtained from Conqwest and subjected to one-step RT-PCR analysis without RNA purification using the FastLane Cell Multiplex Kit (Qiagen, Cat. No. 216513). For transfection, NK-92 cells were collected by centrifugation and diluted with RPMI medium containing 4% FBS and IL2 1000 U/ml and adjusted to 1,000,000 cells/ml.

Multiple sdRNA agents targeting MAP4K4, PPIB or GADPH were diluted separately in serum-free RPMI medium to 4 μM and individually aliquoted at 50 μl/well into a 96-well plate. The prepared cells were then added at 50 μl cells/well to the wells with either MAP4K4, PPIB or GAPDH sdRNAs. Cells were incubated for 24, 48, or 72 hours.

At the specified timepoints, the plated transfected cells were washed once with 100 μl/well PBS and once with FCW buffer. After removal of supernatant, cell processing mix of 23.5 μl FCPL and 1.5 μl gDNA wipeout solution was added to each well and incubated for five minutes at room temperature. Lysates were then transferred to PCR strips and heated at 75° C. for five minutes.

To setup qRT-PCR, the lysates were mixed with QuantiTect reagents from the FastLane Cell Multiplex Kit and with primer probe mix for MAP4K4-FAM/GAPDH-VIC or PPIB-FAM/GAPDH-VIC. The following Taqman gene expression assays were used: human MAP4K4-FAM (Taqman, Hs00377405_ml), human PPIB-FAM (Taqman, Hs00168719_ml) and human GAPDH-VIC (Applied Biosystems, cat. No 4326317E).

A volume of 9 μl/well of each reaction mix was dispensed into a low profile PCR plate. One μl lysate per well was added from the previously prepared lysates. The samples were amplified using the settings recommended by the manufacturer.

Results shown in FIG. 3 demonstrate significant silencing of each of the multiple targets, MAP4K4, PPIB, and GADPH by sdRNA agents transfected into NK-92 cells, including greater than 75% inhibition of expression of each target within 24 to 72 hours of incubation.

Example 5 Silencing of TP53 and MAP4K4 by sdRNA in Human Primary T-Cells

Primary human T-cells were obtained from AllCells (CA) and cultured in complete RPMI medium containing 1000 IU/ml IL2. Cells were activated with anti-CD3/CD28 Dynabeads (Gibco, 11131) according to the manufacturer's instructions for at least 4 days prior to the transfection. Cells were collected by brief vortexing to dislodge the beads from cells and separating them using the designated magnet.

sdRNA agents targeting TP53 or MAP4K4 were prepared by separately diluting the sdRNAs to 0.2-4 μM in serum-free RPMI per sample (well) and individually aliquoted at 100 μl/well of 96-well plate. Cells were prepared in RPMI medium containing 4% FBS and IL2 2000 U/ml at 1,000,000 cells/ml and seeded at 100 μl/well into the 96-well plate with pre-diluted sdRNAs.

At the end of the transfection incubation period, the plated transfected cells were washed once with 100 μl/well PBS and processed with FastLane Cell Multiplex Kit reagents essentially as described for the Example 4 and according to the manufacturer's instructions. Taqman gene expression assays were used in the following combinations: human MAP4K4-FAM/GAPDH-VIC or human TP53-FAM (Taqman, Hs01034249_ml)/GAPDH-VIC. A volume of 18 μl/well of each reaction mix was combined with 2 μl lysates per well from the previously prepared lysates. The samples were amplified as before (see Example 4).

Results shown in FIG. 4 demonstrate significant silencing of both MAP4K4 and TP53 by sdRNA agents transfected into T-cells, reaching 70-80% inhibition of gene expression with 1-2 μM sdRNA.

Example 6 Immunotherapeutic Combination of sdRNAs for Treating Melanoma

Melanomas utilize at least two particular pathways to suppress immune function of T-cells, and each involves both PD1 and CTLA4. Melanoma tumors expressing the PD1 ligand, PD1L, can be targeted with T-cells pretreated ex-vivo with sd-RNAi agents specifically designed to target PD1 and interfere with PD1 expression. PD1 is also known as PDCD1, and particular targeting sequences and gene regions identified and predicted to be particularly functional in sdRNA mediated suppression, are shown in Table 1 for PDCD1 (NM_005018) and for CTLA4 (NM005214).

Treatment of melanoma tumors can be effected by providing to melanoma cells T-cells, such as tumor-infiltrating lymphocytes, pretreated ex-vivo with a combination of sdRNAs targeting PD1/PDCD1 and CTLA4, for example, targeting one or more of the twenty target sequences listed for PD1/PDCD1 and/or CTLA4. A combination of sdRNAs targeting PD1/PDCD1 and FASLG (NM_000639) and/or CTLA4, can increase T-cell toxicity in tumors expressing both PD1L and FAS.

In addition to and in combination with anti-CTLA-4 and anti-PD1 sdRNAs, T-cells used for the immunotherapy of melanoma can also be treated with sdRNA targeting other genes implicated in immunosuppression by the tumor. These receptors include, but are not limited to TGF-beta type 1 and 2 receptors, BTLA (binder of herpes virus entry indicator (HVEM) expressed on melanoma cells), and receptors of integrins expressed by myeloid derived suppressor cells (MDSC), such as CD11b, CD18, and CD29.

For tumors whose profile of expressed suppressive proteins is unknown, any combination of sdRNAs targeting PD1/PDCD1 and any one of know suppressing receptors may be helpful to reduce immune suppression and increase therapeutic efficacy.

Example 7 Combination of sdRNAs for Mitigating Immune Cell Suppression

T-cell or dendritic cell suppression may be modulated by various cytokines, such as IL10 and/or TGF beta. Suppressing corresponding receptors in T-cells and dendritic cells may be beneficial for their activity. For example, providing a combination of anti-PD1 with anti-IL10R sdRNAs is expected to mitigate cytokine induced suppression of T-cells and dendritic cells, as compared with anti-PD1 alone.

Example 8 Combination of sdRNAs for Mitigating Immune Cell Suppression

When the mechanism of tumor suppression of immune cells may be not known, use of sdRNA agents to suppress genes involved in apoptosis (programmed cell death), such as p53, Casp8 or other gene activating apoptosis may be beneficial to increase immune cell activity. Combination of an anti-receptor sdRNAs with sdRNAs against pro-apoptotic genes can additionally reduce death of immune cells and thus increase their activity. For example, combination of anti-PD1 with anti-p53 sdRNAs may additionally protect T-cells from suppression by blocking activation of apoptosis.

Example 9 Silencing of CTLA-4 and PDCD1 by sdRNA in Human Primary T-Cells

Primary human T-cells were cultured and activated essentially as described in Example 5. sdRNA agents targeting PDCD1 and CTLA-4 were prepared by separately diluting the sdRNAs to 0.4-4 μM in serum-free RPMI per sample (well) and aliquoted at 100 μl/well of 96-well plate. Cells were prepared in RPMI medium containing 4% FBS and IL2 2000 U/ml at 1,000,000 cells/ml and seeded at 100 μl/well into the 96-well plate with pre-diluted sdRNAs.

72 h later, the transfected cells were washed once with 100 μl/well PBS and processed with FastLane Cell Multiplex Kit reagents essentially as described for the Example 4 and according to the manufacturer's instructions. Taqman gene expression assays were used in the following combinations: human PDCD1-FAM (Taqman, Hs01550088_ml)/GAPDH-VIC or human CTLA4-FAM (Taqman, Hs03044418_ml)/GAPDH-VIC. A volume of 18 μl/well of each reaction mix was combined with 2 μl lysates per well from the previously prepared lysates. The samples were amplified as before (see Example 4).

Results shown in FIG. 5 demonstrate significant silencing of PDCD1 and CTLA-4 by using combined sdRNA agents delivered to T-cells, obtaining greater than 60-70% inhibition of gene expression with 2 μM sdRNA.

Example 10 Reduction of CTLA-4 and PDCD1 Surface Expression by sdRNA in Human Primary T-Cells

Primary human T-cells were cultured and activated essentially as described in Example 5.

sdRNA agents targeting CTLA-4 or PD1 were separately diluted to 5 μM in serum-free RPMI per sample (well) and aliquoted at 250 μl/well to 24-well plates. Cells mixed with magnetic beads were collected and adjusted to 500,000 cells in 250 μl RPMI medium containing 4% FBS and IL2 2000 IU/ml. Cells were seeded at 250 μl/well to the prepared plate containing pre-diluted sdRNAs. 24 hours later FBS was added to the cells to obtain 10% final concentration.

After 72 hours of incubation, the transfected cells were collected, separated from the activation beads using the magnet, as described in Example 5. Cells were washed with PBS, spun down and resuspended in blocking buffer (PBS with 3% BSA) at 200,000 cells/50 μl/sample.

Antibody dilutions were prepared in the blocking buffer. The antibodies were mixed in two combinations: anti-PD1/anti-CD3 (1:100 dilutions for both antibodies) and anti-CTLA4/anti-CD3 (10 μl/106 cells for anti-CTLA4; 1:100 for CD3). The following antibodies were used: rabbit monoclonal [SP7] to CD3 (Abcam, ab16669); mouse monoclonal [BNI3] to CTLA4 (Abcam, ab33320) and mouse monoclonal [NAT105] to PD1 (Abcam, ab52587). Cells were mixed with the diluted antibodies and incubated 30 minutes on ice. Cells were then washed twice with PBS containing 0.2% Tween-20 and 0.1% sodium azide.

Secondary antibodies were diluted in blocking buffer and mixed together resulting in a final dilution 1:500 for anti-mouse Cy5 (Abcam, ab97037) and 1:2000 for anti-rabbit Alexa-488 (Abcam, ab150077). Cells were mixed with the diluted antibodies at 1:1 ratio and incubated 30 minutes on ice. Cells were washed as before, and diluted in 500 μl PBS per tube. The data was acquired immediately on the Attune Acoustic Focusing Cytometer (Applied Biosystems).

As shown in FIG. 6, sdRNA efficiently reduced surface expression of CTLA-4 and PD1 in activated Human Primary T cells.

Example 11 MAP4K4 sdRNA Delivery into CD3- and CD19-Positive Subsets of Human Peripheral Blood Mononuclear Cells (PBMCs)

PBMCs were cultured in complete RPMI supplemented with 1.5% PHA solution and 500 U/ml IL2. For transfection, PBMCs were collected by centrifugation and diluted with RPMI medium containing 4% FBS and IL2 1000 U/ml and seeded to 24-well plate at 500,000 cells/well.

MAP4K4 sdRNA labeled with cy3 was added to the cells at 0.1 μM final concentration. After 72 hours of incubation, the transfected cells were collected, washed with PBS, spun down and diluted in blocking buffer (PBS with 3% BSA) at 200,000 cells/50 μl/sample.

Antibody dilutions were prepared in the blocking buffer as following: 1:100 final dilution anti-CD3 (Abeam, ab16669) and anti-CD19 at 10 μl/1,000,000 cells (Abeam, ab31947). Cells were mixed with the diluted antibodies and incubated 30 min on ice. Cells were then washed twice with PBS containing 0.2% Tween-20 and 0.1% sodium azide.

Secondary antibodies were diluted in the blocking buffer in a final dilution 1:500 for anti-mouse Cy5 (Abeam, ab97037) and 1:2000 for anti-rabbit Alexa-488 (Abeam, ab150077). Cells were mixed with the diluted antibodies at 1:1 ratio and incubated 30 min on ice. Cells were washed as before, and diluted in 500 μl PBS per tube. The data was acquired immediately on the Attune Acoustic Focusing Cytometer (Applied Biosystems).

FIG. 7 shows efficient transfection over 97% of CD3-positive (t cells) and over 98% CD19-positive (B-cells) subsets in Human Peripheral Blood Mononuclear Cells (PBMCs).

TABLE 1 Targeting sequences and gene regions of genes targeted with sdRNAs to prevent immunosuppression of antigen-presenting cells and T-cells. Accession: HUGO gene symbol: NM_004324 Oligo_ BAX count Oligo_ID targeting sequence Gene_region  1 BAX_NM_004324_human_835 GAATTGCTCAAGTTCATTGA CCTCCACTGCCTCTGGAATTGCTCAAGTTCATTGATGACCCTCTG  2 BAX_NM_004324_human_157 TTCATCCAGGATCGAGCAGG CTTTTGCTTCAGGGTTTCATCCAGGATCGAGCAGGGCGAATGGGG  3 BAX_NM_004324_human_684 ATCATCAGATGTGGTCTATA TCTCCCCATCTTCAGATCATCAGATGTGGTCTATAATGCGTTTTC  4 BAX_NM_004324_human_412 TACTTTGCCAGCAAACTGGT GTTGTCGCCCTTTTCTACTTTGCCAGCAAACTGGTGCTCAAGGCC  5 BAX_NM_004324_human_538 GGTTGGGTGAGACTCCTCAA ATCCAAGACCAGGGTGGTTGGGTGAGACTCCTCAAGCCTCCTCAC  6 BAX_NM_004324_human_411 CTACTTTGCCAGCAAACTGG GGTTGTCGCCCTTTTCTACTTTGCCAGCAAACTGGTGCTCAAGGC  7 BAX_NM_004324_human_706 GCGTTTTCCTTACGTGTCTG GATGTGGTCTATAATGCGTTTTCCTTACGTGTCTGATCAATCCCC  8 BAX_NM_004324_human_716 TACGTGTCTGATCAATCCCC ATAATGCGTTTTCCTTACGTGTCTGATCAATCCCCGATTCATCTA  9 BAX_NM_004324_human_150 TCAGGGTTTCATCCAGGATC AGGGGCCCTTTTGCTTCAGGGTTTCATCCAGGATCGAGCAGGGCG 10 BAX_NM_004324_human_372 TGACGGCAACTTCAACTGGG AGCTGACATGTTTTCTGACGGCAACTTCAACTGGGGCCGGGTTGT 11 BAX_NM_004324_human_356 CAGCTGACATGTTTTCTGAC TCTTTTTCCGAGTGGCAGCTGACATGTTTTCTGACGGCAACTTCA 12 BAX_NM_004324_human_357 AGCTGACATGTTTTCTGACG CTTTTTCCGAGTGGCAGCTGACATGTTTTCTGACGGCAACTTCAA 13 BAX_NM_004324_human_776 CACTGTGACCTTGACTTGAT AGTGACCCCTGACCTCACTGTGACCTTGACTTGATTAGTGCCTTC 14 BAX_NM_004324_human_712 TCCTTACGTGTCTGATCAAT GTCTATAATGCGTTTTCCTTACGTGTCTGATCAATCCCCGATTCA 15 BAX_NM_004324_human_465 GATCAGAACCATCATGGGCT CAAGGTGCCGGAACTGATCAGAACCATCATGGGCTGGACATTGGA 16 BAX_NM_004324_human_642 CTTCTGGAGCAGGTCACAGT TCTGGGACCCTGGGCCTTCTGGAGCAGGTCACAGTGGTGCCCTCT 17 BAX_NM_004324_human_117 TGAGCAGATCATGAAGACAG GGGGCCCACCAGCTCTGAGCAGATCATGAAGACAGGGGCCCTTTT 18 BAX_NM_004324_human_700 TATAATGCGTTTTCCTTACG TCATCAGATGTGGTCTATAATGCGTTTTCCTTACGTGTCTGATCA 19 BAX_NM_004324_human_673 CCCATCTTCAGATCATCAGA CAGTGGTGCCCTCTCCCCATCTTCAGATCATCAGATGTGGTCTAT 20 BAX_NM_004324_human_452 AGGTGCCGGAACTGATCAGA AGGCCCTGTGCACCAAGGTGCCGGAACTGATCAGAACCATCATGG Accession: HUGO gene symbol: NM_001188 Oligo_ BAK1 count Oligo_ID targeting sequence Gene_region  1 BAK1_NM_001188_human_1813 TGGTTTGTTATATCAGGGAA ACAGGGCTTAGGACTTGGTTTGTTATATCAGGGAAAAGGAGTAGG  2 BAK1_NM_001188_human_911 TGGTACGAAGATTCTTCAAA TGTTGGGCCAGTTTGTGGTACGAAGATTCTTCAAATCATGACTCC  3 BAK1_NM_001188_human_1820 TTATATCAGGGAAAAGGAGT TTAGGACTTGGTTTGTTATATCAGGGAAAAGGAGTAGGGAGTTCA  4 BAK1_NM_001188_human_1678 TCCCTTCCTCTCTCCTTATA GTCCTCTCAGTTCTCTCCCTTCCTCTCTCCTTATAGACACTTGCT  5 BAK1_NM_001188_human_926 TCAAATCATGACTCCCAAGG TGGTACGAAGATTCTTCAAATCATGACTCCCAAGGGTGCCCTTTG  6 BAK1_NM_001188_human_1818 TGTTATATCAGGGAAAAGGA GCTTAGGACTTGGTTTGTTATATCAGGGAAAAGGAGTAGGGAGTT  7 BAK1_NM_001188_human_915 ACGAAGATTCTTCAAATCAT GGGCCAGTTTGTGGTACGAAGATTCTTCAAATCATGACTCCCAAG  8 BAK1_NM_001188_human_912 GGTACGAAGATTCTTCAAAT GTTGGGCCAGTTTGTGGTACGAAGATTCTTCAAATCATGACTCCC  9 BAK1_NM_001188_human_2086 GAAGTTCTTGATTCAGCCAA GGGGGTCAGGGGGGAGAAGTTCTTGATTCAGCCAAATGCAGGGAG 10 BAK1_NM_001188_human_620 CCTATGAGTACTTCACCAAG CCACGGCAGAGAATGCCTATGAGTACTTCACCAAGATTGCCACCA 11 BAK1_NM_001188_human_1823 TATCAGGGAAAAGGAGTAGG GGACTTGGTTTGTTATATCAGGGAAAAGGAGTAGGGAGTTCATCT 12 BAK1_NM_001188_human_1687 CTCTCCTTATAGACACTTGC GTTCTCTCCCTTCCTCTCTCCTTATAGACACTTGCTCCCAACCCA 13 BAK1_NM_001188_human_1810 ACTTGGTTTGTTATATCAGG ACTACAGGGCTTAGGACTTGGTTTGTTATATCAGGGAAAAGGAGT 14 BAK1_NM_001188_human_1399 AAGATCAGCACCCTAAGAGA ATTCAGCTATTCTGGAAGATCAGCACCCTAAGAGATGGGACTAGG 15 BAK1_NM_001188_human_654 GTTTGAGAGTGGCATCAATT GATTGCCACCAGCCTGTTTGAGAGTGGCATCAATTGGGGCCGTGT 16 BAK1_NM_001188_human_1875 GACTATCAACACCACTAGGA TCTAAGTGGGAGAAGGACTATCAACACCACTAGGAATCCCAGAGG 17 BAK1_NM_001188_human_1043 AGCTTTAGCAAGTGTGCACT CCTCAAGAGTACAGAAGCTTTAGCAAGTGTGCACTCCAGCTTCGG 18 BAK1_NM_001188_human_1846 TTCATCTGGAGGGTTCTAAG AAAAGGAGTAGGGAGTTCATCTGGAGGGTTCTAAGTGGGAGAAGG 19 BAK1_NM_001188_human_2087 AAGTTCTTGATTCAGCCAAA GGGGTCAGGGGGGAGAAGTTCTTGATTCAGCCAAATGCAGGGAGG 20 BAK1_NM_001188_human_1819 GTTATATCAGGGAAAAGGAG CTTAGGACTTGGTTTGTTATATCAGGGAAAAGGAGTAGGGAGTTC Accession: NM_001228 HUGO gene CASP8 symbol: Oligo_ID targeting sequence Gene_region  1 CASP8_NM_001228_human_2821 TTAAATCATTAGGAATTAAG TCTGCTTGGATTATTTTAAATCATTAGGAATTAAGTTATCTTTAA  2 CASP8_NM_001228_human_2833 GAATTAAGTTATCTTTAAAA ATTTTAAATCATTAGGAATTAAGTTATCTTTAAAATTTAAGTATC  3 CASP8_NM_001228_human_2392 AACTTTAATTCTCTTTCAAA TGTTAATATTCTATTAACTTTAATTCTCTTTCAAAGCTAAATTCC  4 CASP8_NM_001228_human_1683 GACTGAAGTGAACTATGAAG TATTCTCACCATCCTGACTGAAGTGAACTATGAAGTAAGCAACAA  5 CASP8_NM_001228_human_281 ATATTCTCCTGCCTTTTAAA GGGAATATTGAGATTATATTCTCCTGCCTTTTAAAAAGATGGACT  6 CASP8_NM_001228_human_2839 AGTTATCTTTAAAATTTAAG AATCATTAGGAATTAAGTTATCTTTAAAATTTAAGTATCTTTTTT  7  CASP8_NM_001228_human_2164 TAGATTTTCTACTTTATTAA TATTTACTAATTTTCTAGATTTTCTACTTTATTAATTGTTTTGCA  8 CASP8_NM_001228_human_888 CTGTGCCCAAATCAACAAGA CATCCTGAAAAGAGTCTGTGCCCAAATCAACAAGAGCCTGCTGAA  9 CASP8_NM_001228_human_2283 AGCTGGTGGCAATAAATACC TTTGGGAATGTTTTTAGCTGGTGGCAATAAATACCAGACACGTAC 10 CASP8_NM_001228_human_1585 TCCTACCGAAACCCTGCAGA GTGAATAACTGTGTTTCCTACCGAAACCCTGCAGAGGGAACCTGG 11 CASP8_NM_001228_human_2200 TATAAGAGCTAAAGTTAAAT TGTTTTGCACTTTTTTATAAGAGCTAAAGTTAAATAGGATATTAA 12 CASP8_NM_001228_human_2140 CACTATGTTTATTTACTAAT ACTATTTAGATATAACACTATGTTTATTTACTAATTTTCTAGATT 13 CASP8_NM_001228_human_2350 ATTGTTATCTATCAACTATA GGGCTTATGATTCAGATTGTTATCTATCAACTATAAGCCCACTGT 14 CASP8_NM_001228_human_1575 TAACTGTGTTTCCTACCGAA GATGGCCACTGTGAATAACTGTGTTTCCTACCGAAACCCTGCAGA 15 CASP8_NM_001228_human_2397 TAATTCTCTTTCAAAGCTAA ATATTCTATTAACTTTAATTCTCTTTCAAAGCTAAATTCCACACT 16 CASP8_NM_001228_human_2726 TATATGCTTGGCTAACTATA TGCTTTTATGATATATATATGCTTGGCTAACTATATTTGCTTTTT 17 CASP8_NM_001228_human_2805 CTCTGCTTGGATTATTTTAA CATTTGCTCTTTCATCTCTGCTTGGATTATTTTAAATCATTAGGA 18 CASP8_NM_001228_human_2729 ATGCTTGGCTAACTATATTT TTTTATGATATATATATGCTTGGCTAACTATATTTGCTTTTTGCT 19 CASP8_NM_001228_human_2201 ATAAGAGCTAAAGTTAAATA GTTTTGCACTTTTTTATAAGAGCTAAAGTTAAATAGGATATTAAC 20 CASP8_NM_001228_human_2843 ATCTTTAAAATTTAAGTATC ATTAGGAATTAAGTTATCTTTAAAATTTAAGTATCTTTTTTCAAA Accession: HUGO gene symbol: NM_000675 Oligo_ ADORA2A count Oligo_ID targeting sequence Gene_region  1 ADORA2A_NM_000675_human_ TAACTGCCTTTCCTTCTAAA GTGAGAGGCCTTGTCTAACTGCCTTTCCTTCTAAAGGGAATGTTT 2482  2 ADORA2A_NM_000675_human_ TTCCTTCTAAAGGGAATGTT CTTGTCTAACTGCCTTTCCTTCTAAAGGGAATGTTTTTTTCTGAG 2491  3 ADORA2A_NM_000675_human_ GCCTTTCCTTCTAAAGGGAA AGGCCTTGTCTAACTGCCMCCTTCTAAAGGGAATGTTTTTTTTTC 2487  4 ADORA2A_NM_000675_human_ TTTTCTGAGATAAAATAAAA CTAAAGGGAATGTTTTTTTCTGAGATAAAATAAAAACGAGCCACA 2512  5 ADORA2A_NM_000675_human_ CATCTCTTGGAGTGACAAAG TCTCAGTCCCAGGGCCATCTCTTGGAGTGACAAAGCTGGGATCAA 2330  6 ADORA2A_NM_000675_human_ CATGGTGTACTTCAACTTCT GGTCCCCATGAACTACATGGTGTACTTCAACTTCTTTGCCTGTGT 987  7 ADORA2A_NM_000675_human_ CTAACTGCCTTTCCTTCTAA AGTGAGAGGCCTTGTCTAACTGCCTTTCCTTCTAAAGGGAATGTT 2481  8 ADORA2A_NM_000675_human_ CTGATGATTCATGGAGTTTG TGGAGCAGGAGTGTCCTGATGATTCATGGAGTTTGCCCCTTCCTA 1695  9 ADORA2A_NM_000675_human_ CTCAGAGTCCTCTGTGAAAA CCTGGTTTCAGGAGACTCAGAGTCCTCTGTGAAAAAGCCCTTGGA 264 10 ADORA2A_NM_000675_human_ AACGAGCCACATCGTGTTTT CTGAGATAAAATAAAAACGAGCCACATCGTGTTTTAAGCTTGTCC 2531 11 ADORA2A_NM_000675_human_ TCCTTCTAAAGGGAATGTTT TTGTCTAACTGCCTTTCCTTCTAAAGGGAATGTTTTTTTCTGAGA 2492 12 ADORA2A_NM_000675_human_ CATGAACTACATGGTGTACT TGAGGATGTGGTCCCCATGAACTACATGGTGTACTTCAACTTCTT 978 13 ADORA2A_NM_000675_human_ AACTGCCTTTCCTTCTAAAG TGAGAGGCCTTGTCTAACTGCCTTTCCTTCTAAAGGGAATGTTTT 2483 14 ADORA2A_NM_000675_human_ CAGATGTTTCATGCTGTGAG TGGGTTCTGAGGAAGCAGATGTTTCATGCTGTGAGGCCTTGCACC 1894 15 ADORA2A_NM_000675_human_ CCCATGAACTACATGGTGTA TTTGAGGATGTGGTCCCCATGAACTACATGGTGTACTTCAACTTC 976 16 ADORA2A_NM_000675_human_ AGGCAGCAAGAACCTTTCAA CGCAGCCACGTCCTGAGGCAGCAAGAACCTTTCAAGGCAGCTGGC 1384 17 ADORA2A_NM_000675_human_ GTCCTGATGATTCATGGAGT GGATGGAGCAGGAGTGTCCTGATGATTCATGGAGTTTGCCCCTTC 1692 18 ADORA2A_NM_000675_human_ GTACTTCAACTTCTTTGCCT CATGAACTACATGGTGTACTTCAACTTCTTTGCCTGTGTGCTGGT 993 19 ADORA2A_NM_000675_human_ TGTAAGTGTGAGGAAACCCT TTTTTCCAGGAAAAATGTAAGTGTGAGGAAACCCTTTTTATTTTA 2167 20 ADORA2A_NM_000675_human_ CCTACTTTGGACTGAGAGAA TGAGGGCAGCCGGTTCCTACTTTGGACTGAGAGAAGGGAGCCCCA 1815 Accession: HUGO gene NM_005214 symbol: CTLA4  1 CTLA4_NM_005214_human_61 TGATTCTGTGTGGGTTCAAA TCTATATAAAGTCCTTGATTCTGTGTGGGTTCAAACACATTTCAA  2 CTLA4_NM_005214_human_909 TTATTTGTTTGTGCATTTGG GCTATCCAGCTATTTTTATTTGTTTGTGCATTTGGGGGGAATTCA  3 CTLA4_NM_005214_human_1265 TGATTACATCAAGGCTTCAA TCTTAAACAAATGTATGATTACATCAAGGCTTCAAAAATACTCAC  4 CTLA4_NM_005214_human_1094 GATGTGGGTCAAGGAATTAA GGGATGCAGCATTATGATGTGGGTCAAGGAATTAAGTTAGGGAAT  5 CTLA4_NM_005214_human_1241 CCTTTTATTTCTTAAACAAA AAGTTAAATTTTATGCCTTTTATTTCTTAAACAAATGTATGATTA  6 CTLA4_NM_005214_human_1266 GATTACATCAAGGCTTCAAA CTTAAACAAATGTATGATTACATCAAGGCTTCAAAAATACTCACA  7 CTLA4_NM_005214_human_65 TCTGTGTGGGTTCAAACACA TATAAAGTCCTTGATTCTGTGTGGGTTCAAACACATTTCAAAGCT  8 CTLA4_NM_005214_human_1405 TTGATAGTATTGTGCATAGA TATATATATTTTAATTTGATAGTATTGTGCATAGAGCCACGTATG  9 CTLA4_NM_005214_human_1239 TGCCTTTTATTTCTTAAACA TCAAGTTAAATTTTATGCCTTTTATTTCTTAAACAAATGTATGAT 10 CTLA4_NM_005214_human_1912 TCCATGAAAATGCAACAACA TTTAACTCAATATTTTCCATGAAAATGCAACAACATGTATAATAT 11 CTLA4_NM_005214_human_1245 TTATTTCTTAAACAAATGTA TAAATTTTATGCCTTTTATTTCTTAAACAAATGTATGATTACATC 12 CTLA4_NM_005214_human_1449 TTAATGGTTTGAATATAAAC GTTTTTGTGTATTTGTTAATGGTTTGAATATAAACACTATATGGC 13 CTLA4_NM_005214_human_1095 ATGTGGGTCAAGGAATTAAG GGATGCAGCATTATGATGTGGGTCAAGGAATTAAGTTAGGGAATG 14 CTLA4_NM_005214_human_1208 AGCCGAAATGATCTTTTCAA GTATGAGACGTTTATAGCCGAAATGATCTTTTCAAGTTAAATTTT 15 CTLA4_NM_005214_human_1455 GTTTGAATATAAACACTATA GTGTATTTGTTAATGGTTTGAATATAAACACTATATGGCAGTGTC 16 CTLA4_NM_005214_human_1237 TATGCCTTTTATTTCTTAAA TTTCAAGTTAAATTTTATGCCTTTTATTTCTTAAACAAATGTATG 17 CTLA4_NM_005214_human_1911 TTCCATGAAAATGCAACAAC TTTTAACTCAATATTTTCCATGAAAATGCAACAACATGTATAATA 18 CTLA4_NM_005214_human_937 CATCTCTCTTTAATATAAAG CATTTGGGGGGAATTCATCTCTCTTTAATATAAAGTTGGATGCGG 19 CTLA4_NM_005214_human_931 GGAATTCATCTCTCTTTAAT TTTGTGCATTTGGGGGGAATTCATCTCTCTTTAATATAAAGTTGG 20 CTLA4_NM_005214_human_45 ATCTATATAAAGTCCTTGAT TCTGGGATCAAAGCTATCTATATAAAGTCCTTGATTCTGTGTGGG Accession: HUGO gene symbol: NM_002286 Oligo_ LAG3 count Oligo_ID targeting sequence Gene_region  1 LAG3_NM_002286_human_1292 GACTTTACCCTTCGACTAGA ACTGGAGACAATGGCGACTTTACCCTTCGACTAGAGGATGTGAGC  2 LAG3_NM_002286_human_1096 CAACGTCTCCATCATGTATA CTACAGAGATGGCTTCAACGTCTCCATCATGTATAACCTCACTGT  3 LAG3_NM_002286_human_1721 GTCCTTTCTCTGCTCCTTTT TTTCTCATCCTTGGTGTCCTTTCTCTGCTCCTTTTGGTGACTGGA  4 LAG3_NM_002286_human_1465 TCCAGTATCTGGACAAGAAC GCTTTGTGAGGTGACTCCAGTATCTGGACAAGAACGCTTTGTGTG  5 LAG3_NM_002286_human_1795 ATTTTCTGCCTTAGAGCAAG GTGGCGACCAAGACGATTTTCTGCCTTAGAGCAAGGGATTCACCC  6 LAG3_NM_002286_human_1760 TTTCACCTTTGGAGAAGACA ACTGGAGCCTTTGGCTTTCACCTTTGGAGAAGACAGTGGCGACCA  7 LAG3_NM_002286_human_904 CATTTTGAACTGCTCCTTCA AGCCTCCGACTGGGTCATTTTGAACTGCTCCTTCAGCCGCCCTGA  8 LAG3_NM_002286_human_1398 TCATCACAGTGACTCCCAAA CTGTCACATTGGCAATCATCACAGTGACTCCCAAATCCTTTGGGT  9 LAG3_NM_002286_human_1758 GCTTTCACCTTTGGAGAAGA TGACTGGAGCCTTTGGCTTTCACCTTTGGAGAAGACAGTGGCGAC 10 LAG3_NM_002286_human_1753 CTTTGGCTTTCACCTTTGGA TTTGGTGACTGGAGCCTTTGGCTTTCACCTTTGGAGAAGACAGTG 11 LAG3_NM_002286_human_905 ATTTTGAACTGCTCCTTCAG GCCTCCGACTGGGTCATTTTGAACTGCTCCTTCAGCCGCCCTGAC 12 LAG3_NM_002286_human_1387 CACATTGGCAATCATCACAG GCTCAATGCCACTGTCACATTGGCAATCATCACAGTGACTCCCAA 13 LAG3_NM_002286_human_301 TTTCTGACCTCCTTTTGGAG ACTGCCCCCTTTCCTTTTCTGACCTCCTTTTGGAGGGCTCAGCGC 14 LAG3_NM_002286_human_895 CGACTGGGTCATTTTGAACT ATCTCTCAGAGCCTCCGACTGGGTCATTTTGAACTGCTCCTTCAG 15 LAG3_NM_002286_human_1625 TACTTCACAGAGCTGTCTAG CTTGGAGCAGCAGTGTACTTCACAGAGCTGTCTAGCCCAGGTGCC 16 LAG3_NM_002286_human_1390 ATTGGCAATCATCACAGTGA CAATGCCACTGTCACATTGGCAATCATCACAGTGACTCCCAAATC 17 LAG3_NM_002286_human_1703 CTGTTTCTCATCCTTGGTGT GCAGGCCACCTCCTGCTTTTTCTCATCCTTGGTGTCCTTTCTCTG 18 LAG3_NM_002286_human_1453 TTGTGAGGTGACTCCAGTAT CCTGGGGAAGCTGCTTTGTGAGGTGACTCCAGTATCTGGACAAGA 19 LAG3_NM_002286_human_1754 TTTGGCTTTCACCTTTGGAG TTGGTGACTGGAGCCTTTGGCTTTCACCTTTGGAGAAGACAGTGG 20 LAG3_NM_002286_human_1279 TGGAGACAATGGCGACTTTA TGACCTCCTGGTGACTGGAGACAATGGCGACTTTACCCTTCGACT Accession: HUGO gene symbol: NM_005018 Oligo_ PDCD1 count Oligo_ID targeting sequence Gene_region  1 PDCD1_NM_005018_human_2070 TATTATATTATAATTATAAT CCTTCCCTGTGGTTCTATTATATTATAATTATAATTAAATATGAG  2 PDCD1_NM_005018_human_2068 TCTATTATATTATAATTATA CCCCTTCCCTGTGGTTCTATTATATTATAATTATAATTAAATATG  3 POCD1_NM_005018_human_1854 CATTCCTGAAATTATTTAAA GCTCTCCTTGGAACCCATTCCTGAAATTATTTAAAGGGGTTGGCC  4 PDCD1_NM_005018_human_2069 CTATTATATTATAATTATAA CCCTTCCCTGTGGTTCTATTATATTATAATTATAATTAAATATGA  5 PDCD1_NM_005018_human_1491 AGTTTCAGGGAAGGTCAGAA CTGCAGGCCTAGAGAAGTTTCAGGGAAGGTCAGAAGAGCTCCTGG  6 PDCD1_NM_005018_human_2062 TGTGGTTCTATTATATTATA GGGATCCCCCTTCCCTGTGGTTCTATTATATTATAATTATAATTA  7 PDCD1_NM_005018_human_719 TGTGTTCTCTGTGGACTATG CCCCTCAGCCGTGCCTGTGTTCTCTGTGGACTATGGGGAGCTGGA  8 PDCD1_NM_005018_human_1852 CCCATTCCTGAAATTATTTA GAGCTCTCCTTGGAACCCATTCCTGAAATTATTTAAAGGGGTTGG  9 PDCD1_NM_005018_human_812 TGCCACCATTGTCTTTCCTA TGAGCAGACGGAGTATGCCACCATTGTCTTTCCTAGCGGAATGGG 10 PDCD1_NM_005018_human_1490 AAGTTTCAGGGAAGGTCAGA CCTGCAGGCCTAGAGAAGTTTCAGGGAAGGTCAGAAGAGCTCCTG 11 PDCD1_NM_005018_human_2061 CTGTGGTTCTATTATATTAT AGGGATCCCCCTTCCCTGTGGTTCTATTATATTATAATTATAATT 12 PDCD1_NM_005018_human_2067 TTCTATTATATTATAATTAT CCCCCTTCCCTGTGGTTCTATTATATTATAATTATAATTAAATAT 13 PDCD1_NM_005018_human_1493 TTTCAGGGAAGGTCAGAAGA GCAGGCCTAGAGAAGTTTCAGGGAAGGTCAGAAGAGCTCCTGGCT 14 PDCD1_NM_005018_human_1845 CTTGGAACCCATTCCTGAAA ACCCTGGGAGCTCTCCTTGGAACCCATTCCTGAAATTATTTAAAG 15 PDCD1_NM_005018_human_2058 TCCCTGTGGTTCTATTATAT ACAAGGGATCCCCCTTCCCTGTGGTTCTATTATATTATAATTATA 16 PDCD1_NM_005018_human_2060 CCTGTGGTTCTATTATATTA AAGGGATCCCCCTTCCCTGTGGTTCTATTATATTATAATTATAAT 17 PDCD1_NM_005018_human_1847 TGGAACCCATTCCTGAAATT CCTGGGAGCTCTCCTTGGAACCCATTCCTGAAATTATTTAAAGGG 18 PDCD1_NM_005018_human_2055 CCTTCCCTGTGGTTCTATTA GGGACAAGGGATCCCCCTTCCCTGTGGTTCTATTATATTATAATT 19 PDCD1_NM_005018_human_2057 TTCCCTGTGGTTCTATTATA GACAAGGGATCCCCCTTCCCTGTGGTTCTATTATATTATAATTAT 20 PDCD1_NM_005018_human_1105 CACAGGACTCATGTCTCAAT CAGGCACAGCCCCACCACAGGACTCATGTCTCAATGCCCACAGTG Accession: HUGO gene symbol: NM_004612 Oligo_ TGFBR1 count Oligo_ID targeting sequence Gene_region  1 TGFBR1_NM_004612_human_ CCTGTTTATTACAACTTAAA GTTAATAACATTCAACCTGTTTATTACAACTTAAAAGGAACTTCA 5263  2 TGFBR1_NM_004612_human_ CCATTGGTGGAATTCATGAA TTGCTCGACGATGTTCCATTGGTGGAATTCATGAAGATTACCAAC 1323  3 TGFBR1_NM_004612_human_ TTTTCCTTATAACAAAGACA TTTAGGGATTTTTTTTTTTCCTTATAACAAAGACATCACCAGGAT 6389  4 TGFBR1_NM_004612_human_ TGTATTACTTGTTTAATAAT TTTTTATAGTTGTGTTGTATTACTTGTTTAATAATAATCTCTAAT 3611  5 TGFBR1_NM_004612_human_ TTATTGAATCAAAGATTGAG TGCTGAAGATATTTTTTATTGAATCAAAGATTGAGTTACAATTAT 3882  6 TGFBR1_NM_004612_human_ TTCTTACCTAAGTGGATAAA GTTACAATTATACTTTTCTTACCTAAGTGGATAAAATGTACTTTT 3916  7 TGFBR1_NM_004612_human_ ATGTTGCTCAGTTACTCAAA TAAAGTATGGGTATTATGTTGCTCAGTTACTCAAATGGTACTGTA 5559  8 TGFBR1_NM_004612_human_ ATATTTGTACCCCAAATAAC GGTACTGTATTGTTTATATTTGTACCCCAAATAACATCGTCTGTA 5595  9 TGFBR1_NM_004612_human_ TGTAAATGTAAACTTCTAAA TTATGCAATCTTGTTTGTAAATGTAAACTTCTAAAAATATGGTTA 5222 10 TGFBR1_NM_004612_human_ AGAATGAGTGACATATTACA AACCAAAGTAATTTTAGAATGAGTGACATATTACATAGGAATTTA 3435 11 TGFBR1_NM_004612_human_ CCATTTCTAAGCCTACCAGA GTTGTTGTTTTTGGGCCATTTCTAAGCCTACCAGATCTGCTTTAT 3709 12 TGFBR1_NM_004612_human_ ATATTCCAAAAGAATGTAAA ATTGTATTTGTAGTAATATTCCAAAAGAATGTAAATAGGAAATAG 5826 13 TGFBR1_NM_004612_human_ TTACTTCCAATGCTATGAAG TATAATAACTGGTTTTTACTTCCAATGCTATGAAGTCTCTGCAGG 3146 14 TGFBR1_NM_004612_human_ TCTTTATCTGTTCAAAGACT TGTAAGCCATTTTTTTTCTTTATCTGTTCAAAGACTTATTUTTAA 2675 15 TGFBR1_NM_004612_human_ GTCTAAGTATACTTTTAAAA CATTTTAATTGTGTTGTCTAAGTATACTTTTAAAAAATCAAGTGG 2529 16 TGFBR1_NM_004612_human_ ATCTTTGGACATGTACTGCA GAGATACTAAGGATTATCTTTGGACATGTACTGCAGCTTCTTGTC 5079 17 TGFBR1_NM_004612_human_ GTGTTGTATTACTTGTTTAA TTTGTTTTTATAGTTGTGTTGTATTACTTGTTTAATAATAATCTC 3607 18 TGFBR1_NM_004612_human_ TGCTGTAGATGGCAACTAGA CATGCCATATGTAGTTGCTGTAGATGGCAACTAGAACCTTTGAGT 5994 19 TGFBR1_NM_004612_human_ TCTTTCACTTATTCAGAACA GTATACTATTATTGTTCTTTCACTTATTCAGAACATTACATGCCT 2177 20 TGFBR1_NM_004612_human_ GTATTTGTAGTAATATTCCA TTTAAATTGTATATTGTATTTGTAGTAATATTCCAAAAGAATGTA 5814 Accession: HUGO gene symbol: NM _032782 Oligo_ HAVCR2 count Oligo_ID targeting sequence Gene_region  1 HAVCR2_NM_032782_human_937 CTCATAGCAAAGAGAAGATA TTTTCAAATGGTATTCTCATAGCAAAGAGAAGATACAGAATTTAA  2 HAVCR2_NM_032782_human_932 GTATTCTCATAGCAAAGAGA TTTAATTTTCAAATGGTATTCTCATAGCAAAGAGAAGATACAGAA  3 HAVCR2_NM_032782_human_ TTGCTTGTTGTGTGCTTGAA TGTATTGGCCAAGTTTTGCTTGTTGTGTGCTTGAAAGAAAATATC 2126  4 HAVCR2_NM_032782_human_ TATTCGTGGACCAAACTGAA TCTGACCAACTTCTGTATTCGTGGACCAAACTGAAGCTATATTTT 2171  5 HAVCR2_NM_032782_human_158 ATTGTGGAGTAGACAGTTGG GCTACTGCTCATGTGATTGTGGAGTAGACAGTTGGAAGAAGTACC  6 HAVCR2_NM_032782_human_ GTTGTGTGCTTGAAAGAAAA GGCCAAGTTTTGCTTGTTGTGTGCTTGAAAGAAAATATCTCTGAC 2132  7 HAVCR2_NM_032782_human_ TGTTGTGTGCTTGAAAGAAA TGGCCAAGTTTTGCTTGTTGTGTGCTTGAAAGAAAATATCTCTGA 2131  8 HAVCR2_NM_032782_human_ CCCTAAACTTAAATTTCAAG TTGACAGAGAGTGGTCCCTAAACTTAAATTTCAAGACGGTATAGG 2313  9 HAVCR2_NM_032782_human_489 ACATCCAGATACTGGCTAAA GATGTGAATTATTGGACATCCAGATACTGGCTAAATGGGGATTTC 10 HAVCR2_NM_032782_human_ CATTTTCAGAAGATAATGAC GGAGCAGAGTTTTCCCATTTTCAGAAGATAATGACTCACATGGGA 1272 11 HAVCR2_NM_032782_human_785 CACATTGGCCAATGAGTTAC TCTAACACAAATATCCACATTGGCCAATGAGTTACGGGACTCTAG 12 HAVCR2_NM_032782_human_ TGCTTGTTGTGTGCTTGAAA GTATTGGCCAAGTTTTGCTTGTTGTGTGCTTGAAAGAAAATATCT 2127 13 HAVCR2_NM_032782_human_164 GAGTAGACAGTTGGAAGAAG GCTCATGTGATTGTGGAGTAGACAGTTGGAAGAAGTACCCAGTCC 14 HAVCR2_NM_032782_human_ TTGTTGTGTGCTTGAAAGAA TTGGCCAAGTTTTGCTTGTTGTGTGCTTGAAAGAAAATATCTCTG 2130 15 HAVCR2_NM_032782_human_911 CGGCGCTTTAATTTTCAAAT TCTGGCTCTTATCTTCGGCGCTTTAATTTTCAAATGGTATTCTCA 16 HAVCR2_NM_032782_human_ TTTGGCACAGAAAGTCTAAA TGAAAGCATAACTTTTTTGGCACAGAAAGTCTAAAGGGGCCACTG 1543 17 HAVCR2_NM_032782_human_ GATCTGTCTTGCTTATTGTT AGACGGTATAGGCTTGATCTGTCTTGCTTATTGTTGCCCCCTGCG 2346 18 HAVCR2_NM_032782_human_ GGTGTGTATTGGCCAAGTTT GAAGTGCATTTGATTGGTGTGTATTGGCCAAGTTTTGCTTGTTGT 2107 19 HAVCR2_NM_032782_human_ CCCATTTTCAGAAGATAATG ATGGAGCAGAGTTTTCCCATTTTCAGAAGATAATGACTCACATGG 1270 20 HAVCR2_NM_032782_human_ TGGCACAGAAAGTCTAAAGG AAAGCATAALTTTTTTGGCACAGAAAGTCTAAAGGGGCCACTGAT 1545 Accession: HUGO gene symbol: NM _002987 Oligo_ CCL17 count Oligo_ID targeting sequence Gene_region  1 CCL17_NM_002987_human_385 AAATACCTGCAAAGCCTTGA GTGAAGAATGCAGTTAAATACCTGCAAAGCCTTGAGAGGTCTTGA  2 CCL17_NM_002987_human_318 TTTTGTAACTGTGCAGGGCA CAGGGATGCCATCGTTTTTGTAACTGTGCAGGGCAGGGCCATCTG  3 CCL17_NM_002987_human_367 AGAGTGAAGAATGCAGTTAA GACCCCAACAACAAGAGAGTGAAGAATGCAGTTAAATACCTGCAA  4 CCL17_NM_002987_human_396 AAGCCTTGAGAGGTCTTGAA AGTTAAATACCTGCAAAGCCTTGAGAGGTCTTGAAGCCTCCTCAC  5 CCL17_NM_002987_human_386 AATACCTGCAAAGCCTTGAG TGAAGAATGCAGTTAAATACCTGCAAAGCCTTGAGAGGTCTTGAA  6 CCL17_NM_002987_human_378 TGCAGTTAAATACCTGCAAA CAAGAGAGTGAAGAATGCAGTTAAATACCTGCAAAGCCTTGAGAG  7 CCL17_NM_002987_human_357 CAACAACAAGAGAGTGAAGA CATCTGTTCGGACCCCAACAACAAGAGAGTGAAGAATGCAGTTAA  8 CCL17_NM_002987_human_55 CTGAATTCAAAACCAGGGTG CTGCTGATGGGAGAGCTGAATTCAAAACCAGGGTGTCTCCCTGAG  9 CCL17_NM_002987_human_387 ATACCTGCAAAGCCTTGAGA GAAGAATGCAGTTAAATACCTGCAAAGCCTTGAGAGGTCTTGAAG 10 CCL17_NM_002987_human_254 TTCCCCTTAGAAAGCTGAAG ACTTCAAGGGAGCCATTCCCCTTAGAAAGCTGAAGACGTGGTACC 11 CCL17_NM_002987_human_49 GGAGAGCTGAATTCAAAACC CACCGCCTGCTGATGGGAGAGCTGAATTCAAAACCAGGGTGTCTC 12 CCL17_NM_002987_human_379 GCAGTTAAATACCTGCAAAG AAGAGAGTGAAGAATGCAGTTAAATACCTGCAAAGCCTTGAGAGG 13 CCL17_NM_002987_human_372 GAAGAATGCAGTTAAATACC CAACAACAAGAGAGTGAAGAATGCAGTTAAATACCTGCAAAGCCT 14 CCL17_NM_002987_human_377 ATGCAGTTAAATACCTGCAA ACAAGAGAGTGAAGAATGCAGTTAAATACCTGCAAAGCCTTGAGA 15 CCL17_NM_002987_human_252 CATTCCCCTTAGAAAGCTGA GTACTTCAAGGGAGCCATTCCCCTTAGAAAGCTGAAGACGTGGTA 16 CCL17_NM_002987_human_51 AGAGCTGAATTCAAAACCAG CCGCCTGCTGATGGGAGAGCTGAATTCAAAACCAGGGTGTCTCCC 17 CCL17_NM_002987_human_45 GATGGGAGAGCTGAATTCAA GTGTCACCGCCTGCTGATGGGAGAGCTGAATTCAAAACCAGGGTG 18 CCL17_NM_002987_human_44 TGATGGGAGAGCTGAATTCA AGTGTCACCGCCTGCTGATGGGAGAGCTGAATTCAAAACCAGGGT 19 CCL17_NM_002987_human_16 ACTTTGAGCTCACAGTGTCA GCTCAGAGAGAAGTGACTTTGAGCTCACAGTGTCACCGCCTGCTG 20 CCL17_NM_002987_human_368 GAGTGAAGAATGCAGTTAAA ACCCCAACAACAAGAGAGTGAAGAATGCAGTTAAATACCTGCAAA Accession: HUGO gene symbol: NM_002990 Oligo_ CCL22 count Oligo_ID targeting sequence Gene_region  1 CCL22_NM_002990_human_2083 GTATTTGAAAACAGAGTAAA GCTGGAGTTATATATGTATTTGAAAACAGAGTAAATACTTAAGAG  2 CCL22_NM_002990_human_298 CAATAAGCTGAGCCAATGAA GGTGAAGATGATTCTCAATAAGCTGAGCCAATGAAGAGCCTACTC  3 CCL22_NM_002990_human_2103 TACTTAAGAGGCCAAATAGA TGAAAACAGAGTAAATACTTAAGAGGCCAAATAGATGAATGGAAG  4 CCL22_NM_002990_human_2081 ATGTATTTGAAAACAGAGTA AAGCTGGAGTTATATATGTATTTGAAAACAGAGTAAATACTTAAG  5 CCL22_NM_002990_human_2496 TTCATACAGCAAGTATGGGA TTGAGAAATATTCTTTTCATACAGCAAGTATGGGACAGCAGTGTC  6 CCL22_NM_002990_human_1052 CTGCAGACAAAATCAATAAA GAGCCCAGAAAGTGGCTGCAGACAAAATCAATAAAACTAATGTCC  7 CCL22_NM_002990_human_1053 TGCAGACAAAATCAATAAAA AGCCCAGAAAGTGGCTGCAGACAAAATCAATAAAACTAATGTCCC  8 CCL22_NM_002990_human_2112 GGCCAAATAGATGAATGGAA AGTAAATACTTAAGAGGCCAAATAGATGAATGGAAGAATTTTAGG  9 CCL22_NM_002990_human_299 AATAAGCTGAGCCAATGAAG GTGAAGATGATTCTCAATAAGCTGAGCCAATGAAGAGCCTACTCT 10 CCL22_NM_002990_human_2108 AAGAGGCCAAATAGATGAAT ACAGAGTAAATACTTAAGAGGCCAAATAGATGAATGGAAGAATTT 11 CCL22_NM_002990_human_2116 AAATAGATGAATGGAAGAAT AATACTTAAGAGGCCAAATAGATGAATGGAAGAATTTTAGGAACT 12 CCL22_NM_002990_human_2091 AAACAGAGTAAATACTTAAG TATATATGTATTTGAAAACAGAGTAAATACTTAAGAGGCCAAATA 13 CCL22_NM_002990_human_2067 AGCTGGAGTTATATATGTAT TGACTTGGTATTATAAGCTGGAGTTATATATGTATTTGAAAACAG 14 CCL22_NM_002990_human_2047 ACCTTTGACTTGGTATTATA ATGGTGTGAAAGACTACCTTTGACTTGGTATTATAAGCTGGAGTT 15 CCL22_NM_002990_human_238 AACCTTCAGGGATAAGGAGA TGGCGTGGTGTTGCTAACCTTCAGGGATAAGGAGATCTGTGCCGA 16 CCL22_NM_002990_human_2037 GTGAAAGACTACCTTTGACT AATTCATGCTATGGTGTGAAAGACTACCTTTGACTTGGTATTATA 17 CCL22_NM_002990_human_2030 CTATGGTGTGAAAGACTACC ACAATCAAATTCATGCTATGGTGTGAAAGACTACCTTTGACTTGG 18 CCL22_NM_002990_human_1682 CACTACGGCTGGCTAATTTT ATTACAGGTGTGTGCCACTACGGCTGGCTAATTTTTGTATTTTTA 19 CCL22_NM_002990_human_2071 GGAGTTATATATGTATTTGA TTGGTATTATAAGCTGGAGTTATATATGTATTTGAAAACAGAGTA 20 CCL22_NM_002990_human_1111 ATATCAATACAGAGACTCAA CCAAAAGGCAGTTACATATCAATACAGAGACTCAAGGTCACTAGA Accession: HUGO gene symbol: NM_005618 Oligo_ DLL1 count Oligo_ID targeting sequence Gene_region  1 DLL1_NM_005618_human_3246 CTGTTTTGTTAATGAAGAAA TATTTGAGTTTTTTACTGTTTTGTTAATGAAGAAATTCCTTTTTA  2 DIl1_NM_005618_human_3193 TTGTATATAAATGTATTTAT TGTGACTATATTTTTTTGTATATAAATGTATTTATGGAATATTGT  3 DLLl_NM_005618_human_3247 TGTTTTGTTAATGAAGAAAT ATTTGAGTTTTTTTACTGTTTTGTTAATGAAGAAATTCCTTTTAA  4 DLL1_NM_005618_human_3141 AATTTTGGTAAATATGTACA GTTTTTTATAATTTAAATTTTGGTAAATATGTACAAAGGCACTTC  5 DLL1_NM_005618_human_3293 AAATTTTATGAATGACAAAA ATATTTTTCCAAAATAAATTTTATGAATGACAAAAAAAAAAAAAA  6 DLL1_NM_005618_human_3208 TTTATGGAATATTGTGCAAA TTGTATATAAATGTATTTATGGAATATTGTGCAAATGTTATTTGA  7 DLL1_NM_005618_human_3243 TTACTGTTTTGTTAATGAAG TGTTATTTGAGTTTTTTACTGTTTTGTTAATGAAGAAATTCCTTT  8 DLL1_NM_005618_human_2977 TTCTTGAATTAGAAACACAA TTATGAGCCAGTCTTTTCTTGAATTAGAAACACAAACACTGCCTT  9 DLLl_NM_005618_human_2874 CAGTTGCTCTTAAGAGAATA CCGTTGCACTATGGACAGTTGCTCTTAAGAGAATATATATTTAAA 10 DLL1_NM_005618_human_2560 CAACTTCAAAAGACACCAAG CGGACTCGGGCTGTTCAACTTCAAAAGACACCAAGTACCAGTCGG 11 DLL1_NM_005618_human_3285 TCCAAAATAAATTTTATGAA TTTTTAAAATATTTTTCCAAAATAAATTTTATGAATGACAAAAAA 12 DLL1_NM_005618_human_2909 GAACTGAATTACGCATAAGA TATATTTAAATGGGTGAACTGAATTACGCATAAGAAGCATGCACT 13 DLL1_NM_005618_human_1173 GGATTTTGTGACAAACCAGG TGTGATGAGCAGCATGGATTTTGTGACAAACCAGGGGAATGCAAG 14 DLL1_NM_005618_human_3244 TACTGTTTTGTTAATGAAGA GTTATTTGAGTTTTTTACTGTTTTGTTAATGAAGAAATTCCTTTT 15 DLL1_NM_005618_human_3144 TTTGGTAAATATGTACAAAG TTTTATAATTTAAATTTTGGTAAATATGTACAAAGGCACTTCGGG 16 DLL1_NM_005618_human_3286 CCAAAATAAATTTTATGAAT TTTTAAAATATTTTTCCAAAATAAATTTTATGAATGACAAAAAAA 17 DLL1_NM_005618_human_3133 ATAATTTAAATTTTGGTAAA TGATGTTCGTTTTTTATAATTTAAATTTTGGTAAATATGTACAAA 18 DLL1_NM_005618_human_2901 AAATGGGTGAACTGAATTAC AGAGAATATATATTTAAATGGGTGAACTGAATTACGCATAAGAAG 19 DLL1_NM_005618_human_3168 TTCGGGTCTATGTGACTATA TATGTACAAAGGCACTTCGGGTCTATGTGACTATATTTTTTTGTA 20 DLL1_NM_005618_human_3245 ACTGTTTTGTTAATGAAGAA TTAMGAGTMTTACTGTTTTGTTAATGAAGAAATTCCTTTTTTTTT Accession: HUGO gene symbol: NM_000639 Oligo_ FASLG count Oligo_ID targeting sequence Gene_region  1 FASLG_NM_000639_human_1154 TAGCTCCTCAACTCACCTAA GGTTCAAAATGTCTGTAGCTCCTCAACTCACCTAATGTTTATGAG  2 FASLG_NM_000639_human_1771 ATGTTTTCCTATAATATAAT TGTCAGCTACTAATGATGTTTTCCTATAATATAATAAATATTTAT  3 FASLG_NM_000639_human_1774 TTTTCCTATAATATAATAAA CAGCTACTAATGATGTTTTCCTATAATATAATAAATATTTATGTA  4 FASLG_NM_000639_human_1776 TTCCTATAATATAATAAATA GCTACTAATGATGTTTTCCTATAATATAATAAATATTTATGTAGA  5 FASLG_NM_000639_human_1086 TGCATTTGAGGTCAAGTAAG GAGGGTCTTCTTACATGCATTTGAGGTCAAGTAAGAAGACATGAA  6 FASLG_NM_000639_human_1750 ATTGATTGTCAGCTACTAAT TAGTGCTTAAAAATCATTGATTGTCAGCTACTAATGATGTTTTCC  7 FASLG_NM_000639_human_1820 AAATGAAAACATGTAATAAA ATGTGCATTTTTGTGAAATGAAAACATGTAATAAAAAGTATATGT  8 FASLG_NM_000639_human_1659 ATTGTGAAGTACATATTAGG AGAGAGAATGTAGATATTGTGAAGTACATATTAGGAAAATATGGG  9 FASLG_NM_000639_human_667 GCTTTCTGGAGTGAAGTATA CTATGGAATTGTCCTGCTTTCTGGAGTGAAGTATAAGAAGGGTGG 10 FASLG_NM_000639_human_1692 CATTTGGTCAAGATTTTGAA GGAAAATATGGGTTGCATTTGGTCAAGATTTTGAATGCTTCCTGA 11 FASLG_NM_000639_human_986 GGCTTATATAAGCTCTAAGA TCTCAGACGTTTTTCGGCTTATATAAGCTCTAAGAGAAGCACTTT 12 FASLG_NM_000639_human_911 ACCAGTGCTGATCATTTATA GCAGTGTTCAATCTTACCAGTGCTGATCATTTATATGTCAACGTA 13 FASLG_NM_000639_human_598 CCATTTAACAGGCAAGTCCA GCTGAGGAAAGTGGCCCATTTAACAGGCAAGTCCAACTCAAGGTC 14 FASLG_NM_000639_human_1665 AAGTACATATTAGGAAAATA AATGTAGATATTGTGAAGTACATATTAGGAAAATATGGGTTGCAT 15 FASLG_NM_000639_human_1625 TGTGTGTGTGTATGACTAAA GTGTGTGTGTGTGTGTGTGTGTGTGTATGACTAAAGAGAGAATGT 16 FASLG_NM_000639_human_1238 AAGAGGGAGAAGCATGAAAA CTGGGCTGCCATGTGAAGAGGGAGAAGCATGAAAAAGCAGCTACC 17 FASLG_NM_000639_human_1632 GTGTATGACTAAAGAGAGAA TGTGTGTGTGTGTGTGTGTATGACTAAAGAGAGAATGTAGATATT 18 FASLG_NM_000639_human_1581 GTATTTCCAGTGCAATTGTA CCTAACACAGCATGTGTATTTCCAGTGCAATTGTAGGGGTGTGTG 19 FASIG_NM_000639_human_1726 CAACTCTAATAGTGCTTAAA ATGCTTCCTGACAATCAACTCTAATAGTGCTTAAAAATCATTGAT 20 FASLG_NM_000639_human_1626 GTGTGTGTGTATGACTAAAG TGTGTGTGTGTGTGTGTGTGTGTGTATGACTAAAGAGAGAATGTA Accession: HUGO gene symbol: NM_001267706 Oligo_ CD274 count Oligo_ID targeting sequence Gene_region  1 CD274_NM_001267706_human_ ACCTGCATTAATTTAATAAA ATTGTCACTTTTTGTACCTGCATTAATTTAATAAAATATTCTTAT 3222  2 CD274_NM_001267706_human_ AACTTGCCCAAACCAGTAAA GCAAACAGATTAAGTAACTTGCCCAAACCAGTAAATAGCAGACCT 1538  3 CD274_NM_001267706_human_ ATTTGCTCACATCTAGTAAA ACTTGCTGCTTAATGATTTGCTCACATCTAGTAAAACATGGAGTA 1218  4 CD274_NM_001267706_human_ CCTTTGCCATATAATCTAAT TTTATTCCTGATTTGCCTTTGCCATATAATCTAATGCTTGTTTAT 1998  5 CD274_NM_001267706_human_ ATATAGCAGATGGAATGAAT ATTTTAGTGTTTCTTATATAGCAGATGGAATGAATTTGAAGTTCC 2346  6 CD274_NM_001267706_human_ GCCTTTGCCATATAATCTAA ATTTATTCCTGATTTGCCTTTGCCATATAATCTAATGCTTGTTTA 1997  7 CD274_NM_001267706_human_ GATTTGCCTTTGCCATATAA ATTATATTTATTCCTGATTTGCCTTTGCCATATAATCTAATGCTT 1992  8 CD274_NM_001267706_human_ AATTTTCATTTACAAAGAGA CTTAATAATCAGAGTAATTTTCATTTACAAAGAGAGGTCGGTACT 1905  9 CD274_NM_001267706_human_ AGTGTTTCTTATATAGCAGA ATTTTTATTTATTTTAGTGTTTCTTATATAGCAGATGGAATGAAT 2336 10  CD274_NM_001267706_human_ GCTTTCTGTCAAGTATAAAC GAACTTTTGTTTTCTGCTTTCTGTCAAGTATAAACTTCACTTTGA 2656 11  CD274_NM_001267706_human_ CATTTGGAAATGTATGTTAA TCTAAAGATAGTCTACATTTGGAAATGTATGTTAAAAGCACGTAT 2235 12  CD274_NM_001267706_human_ TTATTTTAGTGTTTCTTATA CTTTGCTATTTTTATTTATTTTAGTGTTTCTTATATAGCAGATGG 2329 13  CD274_NM_001267706_human_ GTGGTAGCCTACACACATAA CAGCTTTACAATTATGTGGTAGCCTACACACATAATCTCATTTCA 1433 14  CD274_NM_001267706_human_ ATGAGGAGATTAACAAGAAA GGAGCTCATAGTATAATGAGGAGATTAACAAGAAAATGTATTATT 1745 15  CD274_NM_001267706_human_ CAATTTTGTCGCCAAACTAA TTGTAGTAGATGTTACAATTTTGTCGCCAAACTAAACTTGCTGCT 1183 16  CD274_NM_001267706_human_ TATATAGCAGATGGAATGAA TATTTTAGTGTTTCTTATATAGCAGATGGAATGAATTTGAAGTTC 2345 17  CD274_NM_001267706_human_ AAATGCCACTAAATTTTAAA CTGTCTTTTCTATTTAAATGCCACTAAATTTTAAATTCATACCTT 2069 18  CD274_NM_001267706_human_ TCTTTCCCATAGCTTTTCAT TTTGTTTCTAAGTTATCTTTCCCATAGCTTTTCATTATCTTTCAT 2414 19  CD274_NM_001267706_human_ TATATTCATGACCTACTGGC GATATTTGCTGTCTTTATATTCATGACCTACTGGCATTTGCTGAA 129  20  CD274_NM_001267706_human_ GTCCAGTGTCATAGCATAAG TATTATTACAATTTAGTCCAGTGTCATAGCATAAGGATGATGCGA 1783 Accession: HUGO gene symbol: NM_002164 Oligo_ IDO1 count Oligo_ID targeting sequence Gene_region  1 IDO1_NM_002164_human_1896 ATTCTGTCATAATAAATAAA AAAAAAAAAAGATATATTCTGTCATAATAAATAAAAATGCATAAG  2 IDO1_NM_002164_human_1532 TATCTTATCATTGGAATAAA AAGTTTTGTAATCTGTATCTTATCATTGGAATAAAATGACATTCA  3 IDO1_NM_002164_human_578 GTGATGGAGACTGCAGTAAA TTTTGTTCTCATTTCGTGATGGAGACTGCAGTAAAGGATTCTTCC  4 IDO1_NM_002164_human_1897 TTCTGTCATAATAAATAAAA AAAAAAAAAGATATATTCTGTCATAATAAATAAAAATGCATAAGA  5 IDO1_NM_002164_human_1473 CTTGTAGGAAAACAACAAAA AATACCTdTGCATTTCTTGTAGGAAAACAACAAAAGGTAATTATG  6 IDO1_NM_002164_human_1547 ATAAAATGACATTCAATAAA TATCTTATCATTGGAATAAAATGACATTCAATAAATAAAAATGCA  7 IDO1_NM_002164_human_412 CGTAAGGTCTTGCCAAGAAA GGTCATGGAGATGTCCGTAAGGTCTTGCCAAGAAATATTGCTGTT  8 IDO1_NM_002164_human_1472 TCTTGTAGGAAAACAACAAA AAATACCTGTGCATTTCTTGTAGGAAAACAACAAAAGGTAATTAT  9 IDO1_NM_002164_human_1248 AACTGGAGGCACTGATTTAA ACTGGAAGCCAAAGGAACTGGAGGCACTGATTTAATGAATTTCCT 10 IDO1_NM_002164_human_1440 CAATACAAAAGACCTCAAAA GTTTTACCAATAATGCAATACAAAAGACCTCAAAATACCTGTGCA 11 IDO1_NM_002164_human_636 TGCTTCTGCAATCAAAGTAA GGTGGAAATAGCAGCTGCTTCTGCAATCAAAGTAATTCCTACTGT 12 IDO1_NM_002164_human_1551 AATGACATTCAATAAATAAA TTATCATTGGAATAAAATGACATTCAATAAATAAAAATGCATAAG 13 IDO1_NM_002164_human_1538 ATCATTGGAATAAAATGACA TGTAATCTGTATCTTATCATTGGAATAAAATGACATTCAATAAAT 14 IDO1_NM_002164_human_1430 ACCAATAATGCAATACAAAA ACTATGCAATGTTTTACCAATAATGCAATACAAAAGACCTCAAAA 15 IDO1_NM_002164_human_1527 ATCTGTATCTTATCATTGGA ACTAGAAGTTTTGTAATCTGTATCTTATCATTGGAATAAAATGAC 16 IDO1_NM_002164_human_1533 ATCTTATCATTGGAATAAAA AGTTTTGTAATCTGTATCTTATCATTGGAATAAAATGACATTCAA 17 IDO1_NM_002164_human_632 CAGCTGCTTCTGCAATCAAA TATTGGTGGAAATAGCAGCTGCTTCTGCAATCAAAGTAATTCCTA 18 IDO1_NM_002164_human_1439 GCAATACAAAAGACCTCAAA TGTTTTACCAATAATGCAATACAAAAGACCTCAAAATACCTGTGC 19 IDO1_NM_002164_human_657 TCCTACTGTATTCAAGGCAA TGCAATCAAAGTAATTCCTACTGTATTCAAGGCAATGCAAATGCA 20 IDO1_NM_002164_human_1398 CAGAGCCACAAACTAATACT CATTACCCATTGTAACAGAGCCACAAACTAATACTATGCAATGTT Accession: HUGO gene symbol: NM_001558 Oligo_ IL10RA count Oligo_ID targeting sequence Gene_region  1 IL10RA_NM_001558_human_ TTGTTCATTTATTTATTGGA CTTTATTTATTTATTTTGTTCATTTATTTATTGGAGAGGCAGCAT 3364  2 IL10RA_NM_001558_human_ TTATTCCAATAAATTGTCAA AGTGATACATGTTTTTTATTCCAATAAATTGTCAAGACCACAGGA 3626  3 IL10RA_NM_001558_human_ TATTTTCTGGACACTCAAAC AGATCTTAAGGTATATATTTTCTGGACACTCAAACACATCATAAT 2395  4 IL10RA_NM_001558_human_ TTTATTGGAGAGGCAGCATT TATTTTGTTCATTTATTTATTGGAGAGGCAGCATTGCACAGTGAA 3375  5 IL10RA_NM_001558_human_ ACCTTGGAGAAGTCACTTAT GTTTCCAGTGGTATGACCTTGGAGAAGTCACTTATCCTCTTGGAG 3469  6 IL10RA_NM_001558_human_ TTATTTATTTATTTTGTTCA GTTCCCTTGAAAGCTTTATTTATTTATTTTGTTCATTTATTTATT 3351  7 IL10RA_NM_001558_human_ CTCTTTCCTGTATCATAAAG TCTCCCTCCTAGGAACTCTTTCCTGTATCATAAAGGATTATTTGC 2108  8 IL10RA_NM_001558_human_ CTGAGGAAATGGGTATGAAT GGATGTGAGGTTCTGCTGAGGAAATGGGTATGAATGTGCCTTGAA 3563  9 IL10RA_NM_001558_human_ GAATGTGCCTTGAACACAAA TGAGGAAATGGGTATGAATGTGCCTTGAACACAAAGCTCTGTCAA 3579 10 IL10RA_NM_001558_human_ GGACACTCAAACACATCATA AGGTATATATTTTCTGGACACTCAAACACATCATAATGGATTCAC 2403 11 IL10RA_NM_001558_human_ CTGTATCATAAAGGATTATT CCTAGGAACTCTTTCCTGTATCATAAAGGATTATTTGCTCAGGGG 2115 12 IL10RA_NM_001558_human_ TCACTTCCGAGAGTATGAGA TGAAAGCATCTTCAGTCACTTCCGAGAGTATGAGATTGCCATTCG 563 13 IL10RA_NM_001558_human_ TCTCTGGAGCATTCTGAAAA TCTCAGCCCTGCCTTTCTCTGGAGCATTCTGAAAACAGATATTCT 3197 14 IL10RA_NM_001558_human_ TTATGCCAGAGGCTAACAGA AAGCTGGCTTGTTTCTTATGCCAGAGGCTAACAGATCCAATGGGA 2987 15 IL10RA_NM_001558_human_ AGTGGCATTGACTTAGTTCA AGGGGCCAGGATGACAGTGGCATTGACTTAGTTCAAAACTCTGAG 1278 16 IL10RA_NM_001558_human_ TTTCTGGACACTCAAACACA TCTTAAGGTATATATTTTCTGGACACTCAAACACATCATAATGGA 2398 17 IL10RA_NM_001558_human_ GCATTGCACAGTGAAAGAAT TTTATTGGAGAGGCAGCATTGCACAGTGAAAGAATTCTGGATATC 3390 18 IL10RA_NM_001558_human_ GACCTTGGAGAAGTCACTTA TGTTTCCAGTGGTATGACCTTGGAGAAGTCACTTATCCTCTTGGA 3468 19 IL10RA_NM_001558_human_ TCACGTTCACACACAAGAAA AGGTGCCGGGAAACTTCACGTTCACACACAAGAAAGTAAAACATG 610 20 IL10RA_NM_001558_human_ ACTTTGCTGTTTCCAGTGGT GAAATTCTAGCTCTGACTTTGCTGTTTCCAGTGGTATGACCTTGG 3446 Accession: HUGO gene symbol: NM_000214 Oligo_ JAG1 count Oligo_ID targeting sequence Gene_region  1 JAG1_NM_000214_human_4799 TATTTGATTTATTAACTTAA ATTAATCACTGTGTATATTTGATTTATTAACTTAATAATCAAGAG  2 JAG1_NM_000214_human_5658 GAAAAGTAATATTTATTAAA TTGGCAATAAATTTTGAAAAGTAATATTTATTAAATTTTTTTGTA  3 JAG1_NM_000214_human_4752 ACTTTGTATAGTTATGTAAA AATGTCAAAAGTAGAACTTTGTATAGTTATGTAAATAATTCTTTT  4 JAG1_NM_000214_human_5418 GAATACTTGAACCATAAAAT TCTAATAAGCTAGTTGAATACTTGAACCATAAAATGTCCAGTAAG  5 JAG1_NM_000214_human_5641 TCTTGGCAATAAATTTTGAA TCTTTGATGTGTTGTTCTTGGCAATAAATTTTGAAAAGTAATATT  6 JAG1_NM_000214_human_5150 TTTCTGCTTTAGACTTGAAA TGTTTGTTTTTTGTTTTTCTGCTTTAGACTTGAAAAGAGACAGGC  7 JAG1_NM_000214_human_4526 TATATTTATTGACTCTTGAG GATCATAGTTTTATTTATATTTATTGACTCTTGAGTTGTTTTTGT  8 JAG1_NM_000214_human_4566 TATGATGACGTACAAGTAGT TTTGTATATTGGTTTTATGATGACGTACAAGTAGTTCTGTATTTG  9 JAG1_NM_000214_human_5634 GTGTTGTTCTTGGCAATAAA AAATGCATCTTTGATGTGTTGTTCTTGGCAATAAATTTTGAAAAG 10 JAG1_NM_000214_human_173 CTGATCTAAAAGGGAATAAA CCTTTTTCCATGCAGCTGATCTAAAAGGGAATAAAAGGCTGCGCA 11 JAG1_NM_000214_human_5031 TACGACGTCAGATGTTTAAA GATGGAATTTTTTTGTACGACGTCAGATGTTTAAAACACCTTCTA 12 JAG1_NM_000214_human_4817 AATAATCAAGAGCCTTAAAA TTGATTTATTAACTTAATAATCAAGAGCCTTAAAACATCATTCCT 13 JAG1_NM_000214_human_5685 GTATGAAAACATGGAACAGT TTATTAAATTTTTTTGTATGAAAACATGGAACAGTGTGGCCTCTT 14 JAG1_NM_000214_human_4560 TGGTTTTATGATGACGTACA GTTGTTTTTGTATATTGGTTTTATGATGACGTACAAGTAGTTCTG 15 JAG1_NM_000214_human_5151 TTCTGCTTTAGACTTGAAAA GTTTGTTTTTTGTTTTTCTGCTTTAGACTTGAAAAGAGACAGGCA 16 JAG1_NM_000214_human_5642 CTTGGCAATAAATTTTGAAA CTTTGATGTGTTGTTCTTGGCAATAAATTTTGAAAAGTAATATTT 17 JAG1_NM_000214_human_5377 TTTAATCTACTGCATTTAGG GATTTGATTTTTTTTTTTAATCTACTGCATTTAGGGAGTATTCTA 18 JAG1_NM_000214_human_4756 TGTATAGTTATGTAAATAAT TCAAAAGTAGAACTTTGTATAGTTATGTAAATAATTCTTTTTTAT 19 JAG1_NM_000214_human_4523 ATTTATATTTATTGACTCTT TTAGATCATAGTTTTATTTATATTTATTGACTCTTGAGTTGTTTT 20 JAG1_NM_000214_human_5325 CTTTTCACCATTCGTACATA TGTAAATTCTGATTTCTTTTCACCATTCGTACATAATACTGAACC Accession: HUGO gene symbol: NM_002226 Oligo_ JAG2 count Oligo_ID targeting sequence Gene_region  1 JAG2_NM_002226_human_4266 CGTTTCTTTAACCTTGTATA AATGTTTATTTTCTACGTTTCTTTAACCTTGTATAAATTATTCAG  2 JAG2_NM_002226_human_5800 TAAATGAATGAACGAATAAA GGCAGAACAAATGAATAAATGAATGAACGAATAAAAATTTTGACC  3 JAG2_NM_002226_human_5450 TCATTCATTTATTCCTTTGT GGTCAAAATTTTTATTCATTCATTTATTCCTTTGTTTTGCTTGGT  4 JAG2_NM_002226_human_5021 GTAAATGTGTACATATTAAA TGAAAGTGCATTTTTGTAAATGTGTACATATTAAAGGAAGCACTC  5 JAG2_NM_002226_human_5398 ACCCACGAATACGTATCAAG AGTATAAAATTGCTTACCCACGAATACGTATCAAGGTCTTAAGGA  6 JAG2_NM_002226_human_5371 GTTTTATAAAATAGTATAAA AAACAGCTGAAAACAGTTTTATAAAATAGTATAAAATTGCTTACC  7 JAG2_NM_002226_human_5691 CAACTGAGTCAAGGAGCAAA TGAGGGGTAGGAGGTCAACTGAGTCAAGGAGCAAAGCCAAGAACC  8 JAG2_NM_002226_human_5025 ATGTGTACATATTAAAGGAA AGTGCATTTTTGTAAATGTGTACATATTAAAGGAAGCACTCTGTA  9 JAG2_NM_002226_human_4269 TTCTTTAACCTTGTATAAAT GTTTATTTTCTACGTTTCTTTAACCTTGTATAAATTATTCAGTAA 10 JAG2_NM_002226_human_4258 ATTTTCTACGTTTCTTTAAC AAAAACCAAATGTTTATTTTCTACGTTTCTTTAACCTTGTATAAA 11 JAG2_NM_002226_human_5369 CAGTTTTATAAAATAGTATA TAAAACAGCTGAAAACAGTTTTATAAAATAGTATAAAATTGCTTA 12 JAG2_NM_002226_human_5780 GCACAGGCAGAACAAATGAA GAGTGAGGCTGCCTTGCACAGGCAGAACAAATGAATAAATGAATG 13 JAG2_NM_002226_human_4302 TCAGGCTGAAAACAATGGAG ATTATTCAGTAACTGTCAGGCTGAAAACAATGGAGTATTCTCGGA 14 JAG2_NM_002226_human_5387 TAAAATTGCTTACCCACGAA TTTTATAAAATAGTATAAAATTGCTTACCCACGAATACGTATCAA 15 JAG2_NM_002226_human_4301 GTCAGGCTGAAAACAATGGA AATTATTCAGTAACTGTCAGGCTGAAAACAATGGAGTATTCTCGG 16 JAG2_NM_002226_human_5023 AAATGTGTACATATTAAAGG AAAGTGCATTTTTGTAAATGTGTACATATTAAAGGAAGCACTCTG 17 JAG2_NM_002226_human_4293 CAGTAACTGTCAGGCTGAAA CTTGTATAAATTATTCAGTAACTGTCAGGCTGAAAACAATGGAGT 18 JAG2_NM_002226_human_4321 GTATTCTCGGATAGTTGCTA GCTGAAAACAATGGAGTATTCTCGGATAGTTGCTATTTTTGTAAA 19 JAG2_NM_002226_human_3994 TCTCACACAAATTCACCAAA AGGCGGAGAAGTTCCTCTCACACAAATTCACCAAAGATCCTGGCC 20 JAG2_NM_002226_human_5466 TTGTTTTGCTTGGTCATTCA CATTCATTTATTCCTTTGTTTTGCTTGGTCATTCAGAGGCAAGGT Accession: HUGO gene symbol: NM_001315 Oigo_ MAPK14 count Oligo_ID targeting sequence Gene_region  1 MAPK14_NM_001315_human_670 TCATGCGAAAAGAACCTACA ATTTCAGTCCATCATTCATGCGAAAAGAACCTACAGAGAACTGCG  2 MAPK14_NM_001315_human_833 AAATGTCAGAAGCTTACAGA CTGAACAACATTGTGAAATGTCAGAAGCTTACAGATGACCATGTT  3 MAPK14_NM_001315_human_707 AAACATATGAAACATGAAAA GAACTGCGGTTACTTAAACATATGAAACATGAAAATGTGATTGGT  4 MAPK14_NM_001315_human_863 CAGTTCCTTATCTACCAAAT ACAGATGACCATGTTCAGTTCCTTATCTACCAAATTCTCCGAGGT  5 MAPK14_NM_001315_human_ TCCTGGTACAGACCATATTA TGGAAGAACATTGTTTCCTGGTACAGACCATATTAACCAGCTTCA 1150  6 MAPK14_NM_001315_human_866 TTCCTTATCTACCAAATTCT GATGACCATGTTCAGTTCCTTATCTACCAAATTCTCCGAGGTCTA  7 MAPK14_NM_001315_human_ TTCCTGGTACAGACCATATT CTGGAAGAACATTGTTTCCTGGTACAGACCATATTAACCAGCTTC 1149  8 MAPK14_NM_001315_human_896 AAGTATATACATTCAGCTGA ATTCTCCGAGGTCTAAAGTATATACATTCAGCTGACATAATTCAC  9 MAPK14_NM_001315_human_ CATTACAACCAGACAGTTGA ATGCTGAACTGGATGCATTACAACCAGACAGTTGATATTTGGTCA 1076 10 MAPK14_NM_001315_human_926 AGGGACCTAAAACCTAGTAA GCTGACATAATTCACAGGGACCTAAAACCTAGTAATCTAGCTGTG 11 MAPK14_NM_001315_human_765 CTCTGGAGGAATTCAATGAT TTACACCTGCAAGGTCTCTGGAGGAATTCAATGATGTGTATCTGG 12 MAPK14_NM_001315_human_706 TAAACATATGAAACATGAAA AGAACTGCGGTTACTTAAACATATGAAACATGAAAATGTGATTGG 13 MAPK14_NM_001315_human_815 GATCTGAACAACATTGTGAA CATCTCATGGGGGCAGATCTGAACAACATTGTGAAATGTCAGAAG 14 MAPK14_NM_001315_human_862 TCAGTTCCTTATCTACCAAA TACAGATGACCATGTTCAGTTCCTTATCTACCAAATTCTCCGAGG 15 MAPK14_NM_001315_human_917 ATAATTCACAGGGACCTAAA ATACATTCAGCTGACATAATTCACAGGGACCTAAAACCTAGTAAT 16 MAPK14_NM_001315_human_887 CGAGGTCTAAAGTATATACA ATCTACCAAATTCTCCGAGGTCTAAAGTATATACATTCAGCTGAC 17 MAPK14_NM_001315_human_832 GAAATGTCAGAAGCTTACAG TCTGAACAACATTGTGAAATGTCAGAAGCTTACAGATGACCATGT 18 MAPK14_NM_001315_human_ AGCTGTTGACTGGAAGAACA GATGCATAATGGCCGAGCTGTTGACTGGAAGAACATTGTTTCCTG 1125 19 MAPK14_NM_001315_human_879 AAATTCTCCGAGGTCTAAAG AGTTCCTTATCTACCAAATTCTCCGAGGTCTAAAGTATATACATT 20 MAPK14_NM_001315_human_725 AATGTGATTGGTCTGTTGGA CATATGAAACATGAAAATGTGATTGGTCTGTTGGACGTTTTTACA Accession: HUGO gene NM_003745 symbol: SOCS1  1 SOCS1_NM_003745_human_1141 CTGCTGTGCAGAATCCTATT TCTGGCTTTATTTTTCTGCTGTGCAGAATCCTATTTTATATTTTT  2 SOCS1_NM_003745_human_1143 GCTGTGCAGAATCCTATTTT TGGCTTTATTTTTCTGCTGTGCAGAATCCTATTTTATATTTTTTA  3 SOCS1_NM_003745_human_1170 TTAAAGTCAGTTTAGGTAAT CCTATTTTATATTTTTTAAAGTCAGTTTAGGTAATAAACTTTATT  4 SOCS1_NM_003745_human_1144 CTGTGCAGAATCCTATTTTA GGCTTTATTTTTCTGCTGTGCAGAATCCTATTTTATATTTTTTAA  5 SOCS1_NM_003745_human_1076 GTTTACATATACCCAGTATC CTCCTACCTCTTCATGTTTACATATACCCAGTATCTTTGCACAAA  6 SOCS1_NM_003745_human_837 ATTTTGTTATTACTTGCCTG CTGGGATGCCGTGTTATTTTGTTATTACTTGCCTGGAACCATGTG  7 SOCS1_NM_003745_human_819 TAACTGGGATGCCGTGTTAT CCGTGCACGCAGCATTAACTGGGATGCCGTGTTATTTTGTTATTA  8 SOCSl_NM_003745_human_841 TGTTATTACTTGCCTGGAAC GATGCCGTGTTATTTTGTTATTACTTGCCTGGAACCATGTGGGTA  9 SOCS1_NM_003745_human_1138 TTTCTGCTGTGCAGAATCCT GTCTCTGGCTTTATTTTTCTGCTGTGCAGAATCCTATTTTATATT 10 SOCS1_NM_003745_human_831 CGTGTTATTTTGTTATTACT CATTAACTGGGATGCCGTGTTATTTTGTTATTACTTGCCTGGAAC 11 SOCS1_NM_003745_human_1168 TTTTAAAGTCAGTTTAGGTA ATCCTATTTTATATTTTTTAAAGTCAGTTTAGGTAATAAACTTTA 12 SOCS1_NM_003745_human_1142 TGCTGTGCAGAATCCTATTT CTGGCTTTATTTTTCTGCTGTGCAGAATCCTATTTTATATTTTTT 13 SOCS1_NM_003745_human_825 GGATGCCGTGTTATTTTGTT ACGCAGCATTAACTGGGATGCCGTGTTATTTTGTTATTACTTGCC 14 SOCS1_NM_003745_human_1169 TTTAAAGTCAGTTTAGGTAA TCCTATTTTATATTTTTTAAAGTCAGTTTAGGTAATAAACTTTAT 15 SOCS1_NM_003745_human_1171 TAAAGTCAGTTTAGGTAATA CTATTTTATATTTTTTAAAGTCAGTTTAGGTAATAAACTTTATTA 16 SOCS1_NM_003745_human_1140 TCTGCTGTGCAGAATCCTAT CTCTGGCTTTATTTTTCTGCTGTGCAGAATCCTATTTTATATTTT 17 SOCS1_NM_003745_human_1082 ATATACCCAGTATCTTTGCA CCTCTTCATGTTTACATATACCCAGTATCTTTGCACAAACCAGGG 18 SOCS1_NM_003745_human_1150 AGAATCCTATTTTATATTTT ATTTTTCTGCTGTGCAGAATCCTATTTTATATTTTTTAAAGTCAG 19 SOCS1_NM_003745_human_1011 GGTTGTTGTAGCAGCTTAAC CCTCTGGGTCCCCCTGGTTGTTGTAGCAGCTTAACTGTATCTGGA 20 SOCS1_NM_003745_human_1087 CCCAGTATCTTTGCACAAAC TCATGTTTACATATACCCAGTATCTTTGCACAAACCAGGGGTTGG Accession: HUGO gene symbol: NM_003150 Oligo_ STAT3 count Oligo_ID targeting sequence Gene_region  1 STAT3_NM_003150_human_4897 ATATTGCTGTATCTACTTTA TTTTTTTTTTTTGGTATATTGCTGTATCTACTTTAACTTCCAGAA  2 STAT3_NM_003150_human_4325 TGTTTGTTAAATCAAATTAG GTTTCTGTGGAATTCTGTTTGTTAAATCAAATTAGCTGGTCTCTG  3 STAT3_NM_003150_human_2730 TTTATCTAAATGCAAATAAG TGTGGGTGATCTGCTTTTATCTAAATGCAAATAAGGATGTGTTCT  4 STAT3_NM_003150_human_3615 ATTTTCCTTTGTAATGTATT TTTATAAATAGACTTATTTTCCTTTGTAATGTATTGGCCTTTTAG  5 STAT3_NM_003150_human_453 TATCAGCACAATCTACGAAG GAGTCGAATGTTCTCTATCAGCACAATCTACGAAGAATCAAGCAG  6 STAT3_NM_003150_human_4477 AGCTTAACTGATAAACAGAA CTTCAGTACATAATAAGCTTAACTGATAAACAGAATATTTAGAAA  7 STAT3_NM_003150_human_2870 GTTGTTGTTGTTCTTAGACA CAGCTTTTTGTTATTGTTGTTGTTGTTCTTAGACAAGTGCCTCCT  8 STAT3_NM_003150_human_2873 GTTGTTGTTCTTAGACAAGT CTTTTTGTTATTGTTGTTGTTGTTCTTAGACAAGTGCCTCCTGGT  9 STAT3_NM_003150_human_3096 TCTGTATTTAAGAAACTTAA TATCAGCATAGCCTTTCTGTATTTAAGAAACTTAAGCAGCCGGGC 10 STAT3_NM_003150_human_3613 TTATTTTCCTTTGTAATGTA TTTTTATAAATAGACTTATTTTCCTTTGTAATGTATTGGCCTTTT 11 STAT3_NM_003150_human_4481 TAACTGATAAACAGAATATT AGTACATAATAAGCTTAACTGATAAACAGAATATTTAGAAAGGTG 12 STAT3_NM_003150_human_1372 ACATTCTGGGCACAAACACA GATCCCGGAAATTTAACATTCTGGGCACAAACACAAAAGTGATGA 13 STAT3_NM_003150_human_2720 GTGATCTGCTTTTATCTAAA AATGAGTGAATGTGGGTGATCTGCTTTTATCTAAATGCAAATAAG 14 STAT3_NM_003150_human_1044 CAGACCCGTCAACAAATTAA GCAGAATCTCAACTTCAGACCCGTCAACAAATTAAGAAACTGGAG 15 STAT3_NM_003150_human_1148 GGAGCTGTTTAGAAACTTAA GGAGGAGAGAATCGTGGAGCTGTTTAGAAACTTAATGAAAAGTGC 16 STAT3_NM_003150_human_4523 ACCATTGGGTTTAAATCATA GTGAGACTTGGGCTTACCATTGGGTTTAAATCATAGGGACCTAGG 17 STAT3_NM_003150_human_3573 GGAGAATCTAAGCATTTTAG AATAGGAAGGTTTAAGGAGAATCTAAGCATTTTAGACTTTTTTTT 18 STAT3_NM_003150_human_2987 CCTTGCTGACATCCAAATAG CATTGCACTTTTTAACCTTGCTGACATCCAAATAGAAGATAGGAC 19 STAT3_NM_003150_human_3041 AAATTAAGAAATAATAACAA CCTAGGTTTCTTTTTAAATTAAGAAATAATAACAATTAAAGGGCA 20 STAT3_NM_003150_human_3037 TTTTAAATTAAGAAATAATA AAGCCCTAGGTTTCTTTTTAAATTAAGAAATAATAACAATTAAAG Accession: HUGO gene symbol: NM_006290 Oligo_ TNFAIP3 count Oligo_ID targeting sequence Gene_region  1 TNFAIP3_NM_006290_human_ AGCTTGAACTGAGGAGTAAA ACTTCTAAAGAAGTTAGCTTGAACTGAGGAGTAAAAGTGTGTACA 3451  2 TNFAIP3_NM_006290_human_ CCTTTGCAACATCCTCAGAA AATACACATATTTGTCCTTTGCAACATCCTCAGAAGGCCAATCAT 916  3 TNFAIP3_NM_006290_human_ TTCTTTCCAAAGATACCAAA ACGAATCTTTATAATTTCTTTCCAAAGATACCAAATAAACTTCAG 4422  4 TNFAIP3_NM_006290_human_ TTATTTTATTACAAACTTCA TGTAATTCACTTTATTTATTTTATTACAAACTTCAAGATTATTTA 3688  5 TNFAIP3_NM_006290_human_ TATTTATACTTATTATAAAA GTGAAAAAAAGTAATTATTTATACTTATTATAAAAAGTATTTGAA 4536  6 TNFAIP3_NM_006290_human_ CATTTCAGACAAAATGCTAA AAGGCCAATCATTGTCATTTCAGACAAAATGCTAAGAAGTTTGGA 949  7 TNFAIP3_NM_006290_human_ ATGAAGGAGAAGCTCTTAAA GATCCTGAAAATGAGATGAAGGAGAAGCTCTTAAAAGAGTACTTA 1214  8 TNFAIP3_NM_006290_human_ ATTTTGTGTTGATCATTATT AGTTGATATCTTAATATTTTGTGTTGATCATTATTTCCATTCTTA 4489  9 TNFAIP3_NM_006290_human_ TTCATCGAGTACAGAGAAAA TTTTGCACACTGTGTTTCATCGAGTACAGAGAAAACAAACATTTT 2204 10 TNFAIP3_NM_006290_human_ TTACTGGGAAGACGTGTAAC AAAAATTAGAATATTTTACTGGGAAGACGTGTAACTCTTTGGGTT 3394 11 TNFAIP3_NM_006290_human_ TCATTGAAGCTCAGAATCAG ACTGCCAGAAGTGTTTCATTGAAGCTCAGAATCAGAGATTTCATG 2355 12 TNFAIP3_NM_006290_human_ TTCCATTCTTAATGTGAAAA TGTGTTGATCATTATTTCCATTCTTAATGTGAAAAAAAGTAATTA 4508 13 TNFAIP3_NM_006290_human_ TGAAGGATACTGCCAGAAGT TGGAAGCACCATGTTTGAAGGATACTGCCAGAAGTGTTTCATTGA 2332 14 TNFAIP3_NM_006290_human_ CACAAGAGTCAACATTAAAA ATAAATGTAALTTTTCACAAGAGTCAACATTAAAAAATAAATTAT 4650 15 TNFAIP3_NM_006290_human_ AATTATTTATACTTATTATA AATGTGAAAAAAAGTAATTATTTATACTTATTATAAAAAGTATTT 4533 16 TNFAIP3_NM_006290_human_ TTCGTGCTTCTCCTTATGAA CATATTCATCGATGTTTCGTGCTTCTCCTTATGAAACTCCAGCTA 3907 17 TNFAIP3_NM_006290_human_ TATTTTATTACAAACTTCAA GTAATTCACTTTATTTATTTTATTACAAACTTCAAGATTATTTAA 3689 18 TNFAIP3_NM_006290_human_ TATTACAAACTTCAAGATTA TCACTTTATTTATTTTATTACAAACTTCAAGATTATTTAAGTGAA 3694 19 TNFAIP3_NM_006290_human_ CTCTTAAAGTTGATATCTTA TGTTTTCATCTAATTCTCTTAAAGTTGATATCTTAATATTTTGTG 4467 20 TNFAIP3_NM_006290_human_ TTCCAAAGATACCAAATAAA ATCTTTATAATTTCTTTCCAAAGATACCAAATAAACTTCAGTGTT 4426 Accession: HUGO gene symbol: NM_003326 Oligo_ TNFSF4 count Oligo_ID targeting sequence Gene_region  1 TNFSF4_NM_003326_human_ AATTTGACTTAGCCACTAAC GAGATCAGAATTTTAAATTTGACTTAGCCACTAACTAGCCATGTA 2984  2 TNFSF4_NM_003326_human_ GATATTAATAATATAGTTAA GAGAGTATTAATATTGATATTAATAATATAGTTAATAGTAATATT 3422  3 TNFSF4_NM_003326_human_ CTGTGAATGCACATATTAAA TGCTTACAGTGTTATCTGTGAATGCACATATTAAATGTCTATGTT 3119  4 TNFSF4_NM_003326_human_ GTTTTCTATTTCCTCTTAAG GGATTTTTTTTTCCTGTTTTCTATTTCCTCTTAAGTACACCTTCA 2208  5 TNFSF4_NM_003326_human_ AAATAGCACTAAGAAGTTAT ATTCAATCTGATGTCAAATAGCACTAAGAAGTTATTGTGCCTTAT 1727  6 TNFSF4_NM_003326_human_ CCAATCCCGATCCAAATCAT AATGCTTAAGGGATTCCAATCCCGATCCAAATCATAATTTGTTCT 3311  7 TNFSF4_NM_003326_human_ CTATTTAGAGAATGCTTAAG TTAGTTAGATATTTTCTATTTAGAGAATGCTTAAGGGATTCCAAT 3286  8 TNFSF4_NM_003326_human_ CAGTTTGCATATTGCCTAAA AGGTTAAATTGATTGCAGTTTGCATATTGCCTAAATTTAAACTTT 1222  9 TNFSF4_NM_003326_human_ CTCGAATTCAAAGTATCAAA TATCACATCGGTATCCTCGAATTCAAAGTATCAAAGTACAATTTA 326 10 TNFSF4_NM_003326_human_ ATCTGTGAATGCACATATTA TATGCTTACAGTGTTATCTGTGAATGCACATATTAAATGTCTATG 3117 11 TNFSF4_NM_003326_human_ TTTGTGGGAAAAGAATTGAA TATACATGGCAGAGTTTTGTGGGAAAAGAATTGAATGAAAAGTCA 2938 12 TNFSF4_NM_003326_human_ ATTGACCATGTTCTGCAAAA ATTTCACTTTTTGTTATTGACCATGTTCTGCAAAATTGCAGTTAC 2537 13 TNFSF4_NM_003326_human_ GATTCTTCATTGCAAGTGAA GGTGGACAGGGCATGGATTCTTCATTGCAAGTGAAGGAGCCTCCC 776 14 TNFSF4_NM_003326_human_ GATGTCAAATAGCACTAAGA TATCAAATTCAATCTGATGTCAAATAGCACTAAGAAGTTATTGTG 1721 15 TNFSF4_NM_003326_human_ GTATACAGGGAGAGTGAGAT AAGAGAGATTTTCTTGTATACAGGGAGAGTGAGATAACTTATTGT 1459 16 TNFSF4_NM_003326_human_ GTTGCTATGAGTCAAGGAGT AATGTCTATGTTCTTGTTGCTATGAGTCAAGGAGTGTAACCTTCT 3152 17 TNFSF4_NM_003326_human_ TAGTTGAAATGTCCCCTTAA GTATCCCCTTATGTTTAGTTGAAATGTCCCCTTAACTTGATATAA 1882 18 TNFSF4_NM_003326_human_ CTCTGTGCCAAACCTTTTAT GATGATTTGTAACTTCTCTGTGCCAAACTTTTTATAAACATAAAT 1980 19 TNFSF4_NM_003326_human_ CTCTGTCTAGAAATACCATA ATGAAAAATAATGATCTCTGTCTAGAAATACCATAGACCATATAT 1770 20 TNFSF4_NM_003326_human_ GGTTTCAAGAAATGAGGTGA CACAGAAACATTGCTGGTTTCAAGAAATGAGGTGATCCTATTATC 1680 Accession: HUGO gene symbol: NM_006293 Oligo_ TYRO3 count Oligo_ID targeting sequence Gene_region  1 TYRO3_NM_006293_human_3927 AGTTGCTGTTTAAAATAGAA CATTTCCAAGCTGTTAGTTGCTGTTTAAAATAGAAATAAAATTGA  2 TYRO3_NM_006293_human_3932 CTGTTTAAAATAGAAATAAA CCAAGCTGTTAGTTGCTGTTTAAAATAGAAATAAAATTGAAGACT  3 TYRO3_NM_006293_human_1731 GGCATCAGCGATGAACTAAA ACATTGGACAGCTTGGGCATCAGCGATGAACTAAAGGAAAAACTG  4 TYRO3_NM_006293_human_3699 AATATCCTAAGACTAACAAA GCTACCAAATCTCAAAATATCCTAAGACTAACAAAGGCAGCTGTG  5 TYRO3_NM_006293_human_3928 GTTGCTGTTTAAAATAGAAA ATTTCCAAGCTGTTAGTTGCTGTTTAAAATAGAAATAAAATTGAA  6 TYRO3_NM_006293_human_3938 AAAATAGAAATAAAATTGAA TGTTAGTTGCTGTTTAAAATAGAAATAAAATTGAAGACTAAAGAC  7 TYRO3_NM_006293_human_842 CTGTGAAGCTCACAACCTAA GAGCACCATGTTTTCCTGTGAAGCTCACAACCTAAAAGGCCTGGC  8 TYRO3_NM_006293_human_3953 TTGAAGACTAAAGACCTAAA AAAATAGAAATAAAATTGAAGACTAAAGACCTAAAAAAAAAAAAA  9 TYRO3_NM_006293_human_3703 TCCTAAGACTAACAAAGGCA CCAAATCTCAAAATATCCTAAGACTAACAAAGGCAGCTGTGTCTG 10 TYRO3_NM_006293_human_3909 GGACATTTCCAAGCTGTTAG GGTCCTAGCTGTTAGGGACATTTCCAAGCTGTTAGTTGCTGTTTA 11 TYRO3_NM_006293_human_3190 ATGTTTCCATGGTTACCATG AGGAGTGGGGTGGTTATGTTTCCATGGTTACCATGGGTGTGGATG 12 TYRO3_NM_006293_human_3926 TAGTTGCTGTTTAAAATAGA ACATTTCCAAGCTGTTAGTTGCTGTTTAAAATAGAAATAAAATTG 13 TYRO3_NM_006293_human_3949 AAAATTGAAGACTAAAGACC GTTTAAAATAGAAATAAAATTGAAGACTAAAGACCTAAAAAAAAA 14 TYRO3_NM_006293_human_3900 AGCTGTTAGGGACATTTCCA CATGGGGCGGGTCCTAGCTGTTAGGGACATTTCCAAGCTGTTAGT 15 TYRO3_NM_006293_human_2511 GAGGACGTGTATGATCTCAT CCTCCGGAGTGTATGGAGGACGTGTATGATCTCATGTACCAGTGC 16 TYRO3_NM_006293_human_3400 TTTTAGGTGAGGGTTGGTAA CCTTGTAATATTCCCTTTTAGGTGAGGGTTGGTAAGGGGTTGGTA 17 TYRO3_NM_006293_human_1895 AGCTGACATCATTGCCTCAA TGTGAAGATGCTGAAAGCTGACATCATTGCCTCAAGCGACATTGA 18 TYRO3_NM_006293_human_3690 AAATCTCAAAATATCCTAAG TCTGAGCACGCTACCAAATCTCAAAATATCCTAAGACTAACAAAG 19 TYRO3_NM_006293_human_3919 AAGCTGTTAGTTGCTGTTTA GTTAGGGACATTTCCAAGCTGTTAGTTGCTGTTTAAAATAGAAAT 20 TYRO3_NM_006293_human_3384 TCCTTGTAATATTCCCTTTT AGTCACAAAGAGATGTCCTTGTAATATTCCCTTTTAGGTGAGGGT Accession: HUGO gene symbol: NM_000546 Oligo_ TP53 count Oligo_ID Sequence Gene_region  1 TP53_NM_000546_human_1630 TGTTTGGGAGATGTAAGAAA TTTTACTGTGAGGGATGTTTGGGAGATGTAAGAAATGTTCTTGCA  2 TP53_NM_000546_human_1808 GCATTGTGAGGGTTAATGAA CCTACCTCACAGAGTGCATTGTGAGGGTTAATGAAATAATGTACA  3 TP53_NM_000546_human_2538 TCGATCTCTTATTTTACAAT TATCCCATTTTTATATCGATCTCTTATTTTACAATAAAACTTTGC  4 TP53_NM_000546_human_1812 TGTGAGGGTTAATGAAATAA CCTCACAGAGTGCATTGTGAGGGTTAATGAAATAATGTACATCTG  5 TP53_NM_000546_human_812 GAGTATTTGGATGACAGAAA GGAAATTTGCGTGTGGAGTATTTGGATGACAGAAACACTTTTCGA  6 TP53_NM_000546_human_1627 GGATGTTTGGGAGATGTAAG GGTTTTTACTGTGAGGGATGTTTGGGAGATGTAAGAAATGTTCTT  7 TP53_NM_000546_human_1646 GAAATGTTCTTGCAGTTAAG GTTTGGGAGATGTAAGAAATGTTCTTGCAGTTAAGGGTTAGTTTA  8 TP53_NM_000546_human_1831 ATGTACATCTGGCCTTGAAA AGGGTTAATGAAATAATGTACATCTGGCCTTGAAACCACCTTTTA  9 TP53_NM_000546_human_1645 AGAAATGTTCTTGCAGTTAA TGTTTGGGAGATGTAAGAAATGTTCTTGCAGTTAAGGGTTAGTTT 10 TP53_NM_000546_human_2015 GGTGAACCTTAGTACCTAAA GTCTGACAACCTCTTGGTGAACCTTAGTACCTAAAAGGAAATCTC 11 TP53_NM_000546_human_1753 TAACTTCAAGGCCCATATCT CTGTTGAATTTTCTCTAACTTCAAGGCCCATATCTGTGAAATGCT 12 TP53_NM_000546_human_782 CTTATCCGAGTGGAAGGAAA GCCCCTCCTCAGCATCTTATCCGAGTGGAAGGAAATTTGCGTGTG 13 TP53_NM_000546_human_2086 ATGATCTGGATCCACCAAGA CATCTCTTGTATATGATGATCTGGATCCACCAAGACTTGTTTTAT 14 TP53_NM_000546_human_1744 AATTTTCTCTAACTTCAAGG TGTCCCTCACTGTTGAATTTTCTCTAACTTCAAGGCCCATATCTG 15 TP53_NM_000546_human_2542 TCTCTTATTTTACAATAAAA CCATTTTTATATCGATCTCTTATTTTACAATAAAACTTTGCTGCC 16 TP53_NM_000546_human_2546 TTATTTTACAATAAAACTTT TTTTATATCGATCTCTTATTTTACAATAAAACTTTGCTGCCACCT 17 TP53_NM_000546_human_1842 GCCTTGAAACCACCTTTTAT AATAATGTACATCTGGCCTTGAAACCACCTTTTATTACATGGGGT 18 TP53_NM_000546_human_2534 TATATCGATCTCTTATTTTA TTTATATCCCATTTTTATATCGATCTCTTATTTTACAATAAAACT 19 TP53_NM_000546_human_2021 CCTTAGTACCTAAAAGGAAA CAACCTCTTGGTGAACCTTAGTACCTAAAAGGAAATCTCACCCCA 20 TP53_NM_000546_human_1809 CATTGTGAGGGTTAATGAAA CTACCTCACAGAGTGCATTGTGAGGGTTAATGAAATAATGTACAT 

1. An immune modulator comprising one or more oligonucleotide capable of suppressing expression of a plurality of immune target genes.
 2. An immunogenic composition comprising one or more oligonucleotide, said composition capable of suppressing expression a plurality of target genes in a cell.
 3. The immunogenic composition of claim 2, wherein said composition comprises cells modified to suppress expression of a plurality of immune checkpoint genes.
 4. The immunogenic composition of claim 3, wherein said cells are modified to suppress expression of at least one immune checkpoint gene, and at least one anti-apoptosis gene.
 5. The immunogenic composition of claim 3, wherein said cells are modified to suppress expression of at least one immune checkpoint gene and at least one cytokine receptor gene.
 6. The immunogenic composition of claim 3, wherein said cells are modified to suppress expression of at least one immune checkpoint gene and at least one regulator gene.
 7. The immunogenic composition of claim 3, wherein said cells are modified to suppress expression of a plurality of genes involved in immune suppression, said plurality of genes including at least one target gene listed in Table
 1. 8. The immunogenic composition of claim 3, wherein said cells are modified to suppress expression of a plurality of target genes selected from the group consisting of CTLA4, PD1/PDCD1, TGFBR1, TGFRBR2, IL10RA, TP53, BAX, BAK1, CASP8, ADOARA2A, LAG3, HAVCR2, CCL17, CCL22, DLL2, FASLG, CD274, IDO1, ILIORA, JAG1, JAG2, MAPK14, SOCS1, STAT3, TNFAIP3, and TYRO3, BTLA, KIR, B7-H3 and B7-H4 receptors.
 9. The immunogenic composition of claim 3, wherein said modified cells comprise one or more sdRNAi agents capable of suppressing expression of said plurality of target genes.
 10. The immunogenic composition of claim 9, wherein said cells are selected from the group consisting of T-cells, NK-cells, antigen-presenting cells, dendritic cells, stem cells, induced pluripotent stem cells, and/or stem central memory T-cells.
 11. The immunogenic composition of claim 9, wherein said cells are T-cells comprising one or more transgene expressing high affinity T-cell receptors (TCR) and/or chimeric antibody-T-cell receptors (CAR).
 12. The immunogenic composition of claim 9, wherein said cells comprise one or more sdRNAi agent targeting one or more of: CTLA4, PD1, FAS, TGFR-beta, IL-10R, STAT3, P38, LAG3, TIM3, BTLA, B7-H3 and B7-H4 receptors and adenosine A2a receptor.
 13. The immunogenic composition of claim 9, wherein said cells comprise one or more sdRNAi agent targeting one or more anti-apoptotic genes selected from the group consisting of BAX, BAC, TP53, and Casp8.
 14. The immunogenic composition of claim 9, wherein said sdRNAi agent induces at least 50% inhibition of expression of at least one target gene.
 15. The immunogenic composition of claim 9, wherein said sdRNAi agent comprises at least one 2′-O-methyl modification and/or at least one 2′-O-Fluoro modification, and at least one phosphorothioate modification.
 16. The immunogenic composition of claim 9, wherein said sdRNAi agent comprises at least one hydrophobic modification.
 17. The immunogenic composition of claim 9, wherein said sdRNAi agent is modified to comprises at least one cholesterol molecule.
 18. The immunogenic composition of claim 9, wherein said sdRNA agent is designed to specifically target a gene sequence listed in Table
 1. 19. A method of producing the therapeutic composition comprising one or more oligonucleotide, said composition capable of suppressing expression a plurality of traget genes in a cell, wherein said composition comprises cells modified to suppress expression of a plurality of immune checkpoint genes, said method comprising transforming at least one cell with one or more sdRNA agent capable of targeting and suppressing expression of at least one target gene listed in Table
 1. 20. The method of claim 19, wherein sdRNA inhibit expression of one or more gene selected from the group consisting of: CTLA4, PD1/PDCD1, TGFBR1, TGFRBR2, IL10RA, TP53, BAX, BAK1, CASP8, ADOARA2A, LAG3, HAVCR2, CCL17, CCL22, DLL2, FASLG, CD274, IDO1, ILIORA, JAG1, JAG2, MAPK14, SOCS1, STAT3, TNFAIP3, and TYRO3, BTLA, KIR, B7-H3 and B7-H4 receptors.
 21. The method of claim 19, wherein said cells are selected from the group consisting of T-cells, NK-cells, antigen-presenting cells, dendritic cells, stem cells, induced pluripotent stem cells, and/or stem central memory T-cells.
 22. The method of claim 19, wherein said cells are T-cells comprise one or more transgene expressing high affinity T-cell receptors (TCR) and/or chimeric antibody-T-cell receptors (CAR).
 23. The method of claim 19, wherein said cells are selected from the group consisting of T-cells, NK-cells, antigen-presenting cells, dendritic cells, stem cells, induced pluripotent stem cells, and/or stem central memory T-cells.
 24. (canceled)
 25. A method for treating a subject for suffering from a proliferative disease or infectious disease, the method comprising administering to the subject the therapeutic modulator comprising one or more oligonucleotide capable of suppressing expression of a plurality of immune target genes.
 26. The method of claim 25, wherein said proliferative disease is cancer.
 27. The method of claim 25, wherein said infectious disease is a pathogen infection.
 28. (canceled) 